Containers comprising polyester compositions which comprise cyclobutanediol

ABSTRACT

Described are bottles(s) comprising at least one polyester composition comprising at least one polyester which comprises terephthalic acid residues; 30 to 40 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and 60 to 70 mole % of 1,4-cyclohexanedimethanol residues, wherein the inherent viscosity of said polyester is from 0.50 to 0.68 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at 25° C.; wherein said polyester has a notched Izod impact strength of at least 7.5 ft-lb/inch at 23° C. according to ASTM D256 with a 10-mil notch in a ⅛-inch thick bar; wherein the melt viscosity of said polyester is less than 10,000 poise as measured at 1 radian/second on a rotary melt rheometer at 290° C.; and wherein said polyester composition contains no polycarbonate.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.13/016,147 filed Jan. 28, 2011 which is a continuation of U.S.application Ser. No. 11/390,955 filed on Mar. 28, 2006, which claimspriority under 35 U.S.C. §119(e) to U.S. Provisional Application Ser.No. 60/691,567 filed on Jun. 17, 2005, U.S. Provisional Application Ser.No. 60/731,454 filed on Oct. 28, 2005, U.S. Provisional Application Ser.No. 60/731,389, filed on Oct. 28, 2005, U.S. Provisional ApplicationSer. No. 60/739,058, filed on Nov. 22, 2005, and U.S. ProvisionalApplication Ser. No. 60/738,869, filed on Nov. 22, 2005, U.S.Provisional Application Ser. No. 60/750,692 filed on Dec. 15, 2005, U.S.Provisional Application Ser. No. 60/750,693, filed on Dec. 15, 2005,U.S. Provisional Application Ser. No. 60/750,682, filed on Dec. 15,2005, and U.S. Provisional Application Ser. No. 60/750,547, filed onDec. 15, 2005, all of which are hereby incorporated by this reference intheir entireties.

FIELD OF THE INVENTION

The present invention generally relates to containers comprising apolyester composition made from terephthalic acid, or an ester thereof,or mixtures thereof, 2,2,4,4-tetramethyl-1,3-cyclobutanediol, and1,4-cyclohexanedimethanol, having a certain combination of two or moreof high impact strengths, high glass transition temperature (T_(g)),toughness, certain inherent viscosities, low ductile-to-brittletransition temperatures, good color and clarity, low densities, chemicalresistance, hydrolytic stability, and long crystallization half-times,which allow them to be easily formed into articles.

BACKGROUND OF THE INVENTION

Containers can be produced with a variety of plastic materials by avariety of processes (extrusion blow molding, stretch blow molding,etc.). For example, Polyethylene terephthalate (PET) is a commonmaterial used to make bottles for carbonated soft drinks and water.Unfortunately, PET becomes difficult to use when the fill temperature ofthe container becomes elevated, such as with pasteurization or retortapplications. Higher temperature materials, such as polycarbonate oracrylic polymers, can be made into containers, but the barrier of thesematerials is poor, limiting the types of products that these materialscan contain. Thus, there is a need in the industry for a high-heatmaterial with good barrier that can be fabricated into containers.

Poly(1,4-cyclohexylenedimethylene)terephthalate (PCT), a polyester basedsolely on terephthalic acid or an ester thereof and1,4-cyclohexanedimethanol, is known in the art and is commerciallyavailable. This polyester crystallizes rapidly upon cooling from themelt, making it very difficult to form amorphous articles by methodsknown in the art such as extrusion, injection molding, and the like. Inorder to slow down the crystallization rate of PCT, copolyesters can beprepared containing additional dicarboxylic acids or glycols such asisophthalic acid or ethylene glycol. These ethylene glycol- orisophthalic acid-modified PCTs are also known in the art and arecommercially available.

One common copolyester used to produce films, sheeting, and moldedarticles is made from terephthalic acid, 1,4-cyclohexanedimethanol, andethylene glycol. While these copolyesters are useful in many end-useapplications, they exhibit deficiencies in properties such as glasstransition temperature and impact strength when sufficient modifyingethylene glycol is included in the formulation to provide for longcrystallization half-times. For example, copolyesters made fromterephthalic acid, 1,4-cyclohexanedimethanol, and ethylene glycol withsufficiently long crystallization half-times can provide amorphousproducts that exhibit what is believed to be undesirably higherductile-to-brittle transition temperatures and lower glass transitiontemperatures than the compositions revealed herein.

The polycarbonate of 4,4′-isopropylidenediphenol (bisphenol Apolycarbonate) has been used as an alternative for polyesters known inthe art and is a well known engineering molding plastic. Bisphenol Apolycarbonate is a clear, high-performance plastic having good physicalproperties such as dimensional stability, high heat resistance, and goodimpact strength. Although bisphenol-A polycarbonate has many goodphysical properties, its relatively high melt viscosity leads to poormelt processability and the polycarbonate exhibits poor chemicalresistance. It is also difficult to thermoform.

Polymers containing 2,2,4,4-tetramethyl-1,3-cyclobutanediol have alsobeen generally described in the art. Generally, however, these polymersexhibit high inherent viscosities, high melt viscosities and/or high Tgs(glass transition temperatures) such that the equipment used in industrycan be insufficient to manufacture or post polymerization process thesematerials.

Thus, there is a need in the art for containers comprising at least onepolymer having a combination of two or more properties, chosen from atleast one of the following: toughness, high glass transitiontemperatures, high impact strength, hydrolytic stability, chemicalresistance, long crystallization half-times, low ductile to brittletransition temperatures, good color, and clarity, lower density and/orthermoformability of polyesters while retaining processability on thestandard equipment used in the industry.

SUMMARY OF THE INVENTION

It is believed that certain containers comprising polyester compositionsformed from terephthalic acid, an ester thereof, or mixtures thereof,1,4-cyclohexanedimethanol and 2,2,4,4-tetramethyl-1,3-cyclobutanediolwith certain monomer compositions, inherent viscosities and/or glasstransition temperatures are superior to polyesters known in the art andto polycarbonate with respect to one or more of high impact strengths,hydrolytic stability, toughness, chemical resistance, good color andclarity, long crystallization half-times, low ductile to brittletransition temperatures, lower specific gravity, and thermoformability.These compositions are believed to be similar to polycarbonate in heatresistance and are still processable on the standard industry equipment.

In one aspect, the invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.10 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,

(c) residues from at least one branching agent;

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %; and

wherein the inherent viscosity of the polyester is from 0.35 to 1.2 dL/gas determined in 60/40 (wt/wt)phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the polyester has aTg of 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 80 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 20 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 85° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 80 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 20 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 125 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to less than 80 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) greater than 20 to 60 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 125 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 55 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 45 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; wherein the        polyester has a Tg of 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 50 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 45 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; wherein the        polyester has a Tg of 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 45 to 55 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 45 to 55 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; wherein the        polyester has a Tg of 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 50 up to 99 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 1 to less than 50 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 50 up to 80 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 20 to less than 50 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 85° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 51 up to 80 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 20 to less than 49 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 85° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,

(c) residues of at least one branching agent;

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %; and

wherein the inherent viscosity of the polyester is from 0.35 to 1.2 dL/gas determined in 60/40 (wt/wt)phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the polyester has aTg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 50 up to 99 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 1 to less than 50 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 110° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 51 up to 99 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 1 to less than 49 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 110° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 50 up to 80 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 20 to less than 50 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 110° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 51 up to 80 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 20 to less than 49 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 110° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of from 110 to 200°        C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 80 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 20 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to less than 80 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) greater than 20 to 60 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 55 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 50 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 50 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 50 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 45 to 55 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 45 to 55 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 80 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 20 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 and        less than 0.70 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of from 110 to 200°        C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is greater than        0.76 up to 1.2 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of from 110° C. to        200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 110 to 150° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 110 to 150° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 120 to 135° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 120 to 135° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 127° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 80 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 20 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 127° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from greater than 148° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from greater than 148° C. to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 64.9 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35.1 to 59.1 mole % of 1,4-cyclohexanedimethanol residues,    -   iii) 0.10 to less than 15 mole % ethylene glycol residues;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; wherein the        polyester has a Tg of 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 85 to 200° C. and        optionally, wherein one or more branching agents is added prior        to or during the polymerization of the polymer.

In one aspect, this invention relates to a container comprising:

(I) at least one polyester composition comprising at least one polyesterwhich comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and        (II) at least one thermal stabilizer and/or reaction products        thereof;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethane at a        concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 85 to 200° C.

In one aspect, this invention relates to a container comprising:

(I) at least one polyester composition comprising at least one polyesterwhich comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues; and        (II) at least one thermal stabilizer and/or reaction products        thereof;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethane at a        concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 85 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 64.9 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 59.9 mole % of 1,4-cyclohexanedimethanol        residues, iii) 0.10 to less than 15 mole % ethylene glycol        residues;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 035 to        0.75 dL/g or less as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues; and        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 0.75        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 110 to 200° C. and        optionally, wherein one or more branching agents is added prior        to or during the polymerization of the polymer.

In one aspect, this invention relates to a container comprising:

(I) at least one polyester composition comprising at least one polyesterwhich comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues;        (II) at least one thermal stabilizer and/or reaction products        thereof;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethane at a        concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising:

(I) at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues; and        (II) at least one thermal stabilizer and/or reaction products        thereof;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethane at a        concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising:

(I) at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 64.9 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35.1 to 60 mole % of 1,4-cyclohexanedimethanol residues,    -   iii) 0.10 to less than 15 mole % ethylene glycol residues;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 035 to        0.75 dL/g or less as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 0.75        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 110 to 200° C. and        optionally, wherein one or more branching agents is added prior        to or during the polymerization of the polymer.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,

(c) residues of at least one branching agent;

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %; and

wherein the inherent viscosity of the polyester is from 0.35 to 1.2 dL/gas determined in 60/40 (wt/wt)phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the polyester has aTg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and        (II) at least thermal stabilizer and/or reaction products        thereof;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethane at a        concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising:

(I) at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 40 to 65 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 35 to 60 mole % of 1,4-cyclohexanedimethanol residues; and        (II) at least one thermal stabilizer and/or reaction products        thereof;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethane at a        concentration of 0.5 g/100 ml at 25° C.;        wherein the polyester has a Tg of 110 to 200° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) greater than 40 to 99 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) 1 to less than 60 mole % of 1,4-cyclohexanedimethanol        residues;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.10 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; wherein the        polyester has a Tg of 85 to 200° C.; wherein the polyester is        amorphous; wherein if ethylene glycol residues is present in the        glycol component, it is present in the amount of 0.01 to less        than 15 mole %.

In one aspect, this invention relates to a container comprising anamorphous polyester comprising:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 10 to 100 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 0 to 90 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %.

In one aspect, this invention relates to a container comprising anamorphous polyester comprising:

(a) a dicarboxylic acid component comprising:

-   -   i) 90 to 100 mole % of terephthalic acid residues;    -   ii) up to 10 mole % of aromatic dicarboxylic acid residues        having up to 20 carbon atoms; and    -   iii) up to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) from 25 to 100 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) up to 75 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and wherein the amorphous polyester has a glass        transition temperature (T_(g)) of greater than 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.10 to less        than 1 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of from 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to 1.2        dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at        a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of from 95° C. to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is 0.35 to less        than 1 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of from 95° C. to        115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 5 to less than 50 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) greater than 50 to 95 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 10 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 70 to 90 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 3 to 10 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 90 to 97 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 3 to 10 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 90 to 97 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from greater        than 0.60 to 1.2 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 3 to 9 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 91 to 97 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 8 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 92 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 7 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 93 to 99 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 11 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 70 to 89 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 12 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 70 to 88 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 13 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 70 to 87 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 14 to 25 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 75 to 86 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity is from 0.35 to 1.2 dL/g as        determined in 60/40 (wt/wt) phenol/tetrachloroethane at a        concentration of 0.5 g/100 ml at 25° C.; and        wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 5 to less than 50 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) greater than 50 to 95 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 95 to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 10 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 70 to 90 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 95 to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 14 to 25 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 75 to 86 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 95 to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 5 to less than 50 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) greater than 50 to 95 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        less than 0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 10 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 70 to 90 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        less than 0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 14 to 25 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 75 to 86 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        less than 0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 85 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 5 to less than 50 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and    -   ii) greater than 50 to 95 mole % of 1,4-cyclohexanedimethanol        residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        less than 0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 95 to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 10 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 70 to 90 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        less than 0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 95 to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 14 to 25 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 75 to 86 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.50 to        less than 0.75 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 95 to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 14 to 25 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; and    -   ii) 75 to 86 mole % of 1,4-cyclohexanedimethanol residues,        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.6 to        0.72 dL/g as determined in 60/40 (wt/wt)        phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at        25° C.; and wherein the polyester has a Tg of 95 to 115° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to less than 5 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues;    -   ii) ethylene glycol residues, and    -   iii) optionally, 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 4.5 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) optionally, 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 4 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) optionally, 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 3 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 2 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) optionally, 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 1 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to less than 1 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 15 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 15 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) 70 to 99.98 mole % ethylene glycol residues, and    -   iii) 0.01 to 15 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 10 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 10 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues; ii) 80 to 99.98 mole % of ethylene glycol residues,        and    -   iii) 0.01 to 10 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 5 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to less than 5 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 4.5 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 4 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 3 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 2.0 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 1 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to less than 1 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues;    -   ii) ethylene glycol residues, and    -   iii) 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

A container comprising at least one polyester composition comprising atleast one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 5 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) 90 to 99.98 mole % of ethylene glycol residues, and    -   iii) 0.01 to 5 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to less than 5 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues;    -   ii) greater than 90 to 99.98 mole % of ethylene glycol residues,        and    -   iii) 0.01 to 5 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 4 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) 91 to 99.98 mole % of ethylene glycol residues, and    -   iii) 0.01 to 5 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 3 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) 92 to 99.98 mole % of ethylene glycol residues, and    -   iii) 0.01 to 5 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 2 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) 93 to 99.98 mole % of ethylene glycol residues, and    -   iii) 0.01 to 5 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 1 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol        residues;    -   ii) 94 to 99.98 mole % of ethylene glycol residues, and    -   iii) 0.01 to 5 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, this invention relates to a container comprising at leastone polyester composition comprising at least one polyester whichcomprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of terephthalic acid residues;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 10 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to less than 1 mole % of        2,2,4,4-tetramethyl-1,3-cyclobutanediol residues;    -   ii) greater than 94 to 99.98 mole % of ethylene glycol residues,        and    -   iii) 0.01 to 5 mole % of 1,4-cyclohexanedimethanol residues        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %; and        wherein the inherent viscosity of the polyester is from 0.35 to        1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane        at a concentration of 0.5 g/100 ml at 25° C.; and wherein the        polyester has a Tg of 60 to 120° C.

In one aspect, the polyester compositions of the invention contain atleast one polycarbonate.

In one aspect, the polyester compositions of the invention contain nopolycarbonate.

In one aspect, the polyesters useful in the invention contain less than15 mole % ethylene glycol residues, such as, for example, 0.01 to lessthan 15 mole % ethylene glycol residues.

In one aspect, the polyesters useful in the invention contain noethylene glycol residues.

In one aspect the polyester compositions useful in the invention containat least one thermal stabilizer and/or reaction products thereof.

In one aspect, the polyesters useful in the invention contain nobranching agent, or alternatively, at least one branching agent is addedeither prior to or during polymerization of the polyester.

In one aspect, the polyesters useful in the invention contain at leastone branching agent without regard to the method or sequence in which itis added.

In one aspect, the polyesters useful in the invention are made from no1,3-propanediol, or, 1,4-butanediol, either singly or in combination. Inother aspects, 1,3-propanediol or 1,4-butanediol, either singly or incombination, may be used in the making of the polyesters useful in thisinvention.

In one aspect of the invention, the mole % ofcis-2,2,4,4-tetramethyl-1,3-cyclobutanediol useful in certain polyestersuseful in the invention is greater than 50 mole % or greater than 55mole % of cis-2,2,4,4-tetramethyl-1,3-cyclobutanediol or greater than 70mole % of cis-2,2,4,4-tetramethyl-1,3-cyclobutanediol; wherein the totalmole percentage of cis-2,2,4,4-tetramethyl-1,3-cyclobutanediol andtrans-2,2,4,4-tetramethyl-1,3-cyclobutanediol is equal to a total of 100mole %.

In one aspect of the invention, the mole % of the isomers of2,2,4,4-tetramethyl-1,3-cyclobutanediol useful in certain polyestersuseful in the invention is from 30 to 70 mole % ofcis-2,2,4,4-tetramethyl-1,3-cyclobutanediol or from 30 to 70 mole % oftrans-2,2,4,4-tetramethyl-1,3-cyclobutanediol, or from 40 to 60 mole %of cis-2,2,4,4-tetramethyl-1,3-cyclobutanediol or from 40 to 60 mole %of trans-2,2,4,4-tetramethyl-1,3-cyclobutanediol, wherein the total molepercentage of cis-2,2,4,4-tetramethyl-1,3-cyclobutanediol andtrans-2,2,4,4-tetramethyl-1,3-cyclobutanediol is equal to a total of 100mole %.

In one aspect, the polyester compositions are useful in containersincluding but not limited to extruded, calendered, and/or moldedarticles including but not limited to injection molded articles,thermoformed articles, extruded articles, cast extrusion articles,profile extrusion articles, extrusion molded articles, injection blowmolded articles, injection stretch blow molded articles, extrusion blowmolded articles and extrusion stretch blow molded articles. Thesecontainers can include but are not limited to bottles.

Also, in one aspect, use of these particular polyester compositionsminimizes and/or eliminates the drying step prior to melt processingand/or thermoforming.

In one aspect, certain polyesters useful in the invention may beamorphous or semicrystalline. In one aspect, certain polyesters usefulin the invention can have a relatively low crystallinity. Certainpolyesters useful in the invention can thus have a substantiallyamorphous morphology, meaning that the polyesters comprise substantiallyunordered regions of polymer.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph showing the effect of comonomer on the fastestcrystallization half-times of modified PCT copolyesters.

FIG. 2 is a graph showing the effect of comonomer on thebrittle-to-ductile transition temperature (T_(bd)) in a notched Izodimpact strength test (ASTM D256, ⅛-in thick, 10-mil notch).

FIG. 3 is a graph showing the effect of2,2,4,4-tetramethyl-1,3-cyclobutanediol composition on the glasstransition temperature (Tg) of the copolyester.

DETAILED DESCRIPTION OF THE INVENTION

The present invention may be understood more readily by reference to thefollowing detailed description of certain embodiments of the inventionand the working examples. In accordance with the purpose(s) of thisinvention, certain embodiments of the invention are described in theSummary of the Invention and are further described herein below. Also,other embodiments of the invention are described herein.

It is believed that polyesters and/or polyester composition(s) which areincluded in the containers of the invention can have a uniquecombination of two or more physical properties such as moderate or highimpact strengths, high glass transition temperatures, chemicalresistance, hydrolytic stability, toughness, low ductile-to-brittletransition temperatures, good color and clarity, low densities, and longcrystallization half-times, and good processability thereby easilypermitting them to be formed into articles. In some of the embodimentsof the invention, the polyesters have a unique combination of theproperties of good impact strength, heat resistance, chemicalresistance, density and/or the combination of the properties of goodimpact strength, heat resistance, and processability and/or thecombination of two or more of the described properties, that have neverbefore been believed to be present in containers comprising thepolyester compositions which comprise the polyester(s) as disclosedherein.

The term “container” as used herein is understood to mean a receptaclein which material is held or stored. “Containers” include but are notlimited to bottles, bags, vials, tubes and jars. Applications in theindustry for these types of containers include but are not limited tofood, beverage, cosmetics and personal care applications.

The term “bottle” as used herein is understood to mean a receptaclecontaining plastic which is capable of storing or holding liquid.

The term “polyester”, as used herein, is intended to include“copolyesters” and is understood to mean a synthetic polymer prepared bythe reaction of one or more difunctional carboxylic acids and/ormultifunctional carboxylic acids with one or more difunctional hydroxylcompounds and/or multifunctional hydroxyl compounds. Typically thedifunctional carboxylic acid can be a dicarboxylic acid and thedifunctional hydroxyl compound can be a dihydric alcohol such as, forexample, glycols and diols. The term: “glycol” as used herein includes,but is not limited to, diols, glycols, and/or multifunctional hydroxylcompounds, for example, branching agents Alternatively, the difunctionalcarboxylic acid may be a hydroxy carboxylic acid such as, for example,p-hydroxybenzoic acid, and the difunctional hydroxyl compound may be anaromatic nucleus bearing 2 hydroxyl substituents such as, for example,hydroquinone. The term “residue”, as used herein, means any organicstructure incorporated into a polymer through a polycondensation and/oran esterification reaction from the corresponding monomer. The term“repeating unit”, as used herein, means an organic structure having adicarboxylic acid residue and a diol residue bonded through acarbonyloxy group. Thus, for example, the dicarboxylic acid residues maybe derived from a dicarboxylic acid monomer or its associated acidhalides, esters, salts, anhydrides, or mixtures thereof. Furthermore, asused herein, the term “diacid” includes multifunctional acids, forexample, branching agents. As used herein, therefore, the term“dicarboxylic acid” is intended to include dicarboxylic acids and anyderivative of a dicarboxylic acid, including its associated acidhalides, esters, half-esters, salts, half-salts, anhydrides, mixedanhydrides, or mixtures thereof, useful in a reaction process with adiol to make polyester. As used herein, the term “terephthalic acid” isintended to include terephthalic acid itself and residues thereof aswell as any derivative of terephthalic acid, including its associatedacid halides, esters, half-esters, salts, half-salts, anhydrides, mixedanhydrides, or mixtures thereof or residues thereof useful in a reactionprocess with a diol to make polyester.

In one embodiment, terephthalic acid may be used as the startingmaterial. In another embodiment, dimethyl terephthalate may be used asthe starting material. In yet another embodiment, mixtures ofterephthalic acid and dimethyl terephthalate may be used as the startingmaterial and/or as an intermediate material.

The polyesters used in the present invention typically can be preparedfrom dicarboxylic acids and diols which react in substantially equalproportions and are incorporated into the polyester polymer as theircorresponding residues. The polyesters of the present invention,therefore, can contain substantially equal molar proportions of acidresidues (100 mole %) and diol (and/or multifunctional hydroxylcompound) residues (100 mole %) such that the total moles of repeatingunits is equal to 100 mole %. The mole percentages provided in thepresent disclosure, therefore, may be based on the total moles of acidresidues, the total moles of diol residues, or the total moles ofrepeating units. For example, a polyester containing 30 mole %isophthalic acid, based on the total acid residues, means the polyestercontains 30 mole % isophthalic acid residues out of a total of 100 mole% acid residues. Thus, there are 30 moles of isophthalic acid residuesamong every 100 moles of acid residues. In another example, a polyestercontaining 30 mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol, based onthe total diol residues, means the polyester contains 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues out of a total of 100mole % diol residues. Thus, there are 30 moles of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues among every 100 molesof diol residues.

In other aspects of the invention, the Tg of the polyesters useful inthe bottle(s) of the invention can be at least one of the followingranges: 60 to 200° C.; 60 to 190° C.; 60 to 180° C.; 60 to 170° C.; 60to 160° C.; 60 to 155° C.; 60 to 150° C.; 60 to 145° C.; 60 to 140° C.;60 to 138° C.; 60 to 135° C.; 60 to 130° C.; 60 to 125° C.; 60 to 120°C.; 60 to 115° C.; 60 to 110° C.; 60 to 105° C.; 60 to 100° C.; 60 to95° C.; 60 to 90° C.; 60 to 85° C.; 60 to 80° C.; 60 to 75° C.; 65 to200° C.; 65 to 190° C.; 65 to 180° C.; 65 to 170° C.; 65 to 160° C.; 65to 155° C.; 65 to 150° C.; 65 to 145° C.; 65 to 140° C.; 65 to 138° C.;65 to 135° C.; 65 to 130° C.; 65 to 125° C.; 65 to 120° C.; 65 to 115°C.; 65 to 110° C.; 65 to 105° C.; 65 to 100° C.; 65 to 95° C.; 65 to 90°C.; 65 to 85° C.; 65 to 80° C.; 65 to 75° C.; 70 to 200° C.; 70 to 190°C.; 70 to 180° C.; 70 to 170° C.; 70 to 160° C.; 70 to 155° C.; 70 to150° C.; 70 to 145° C.; 70 to 140° C.; 70 to 138° C.; 70 to 135° C.; 70to 130° C.; 70 to 125° C.; 70 to 120° C.; 70 to 115° C.; 70 to 110° C.;70 to 105° C.; 70 to 100° C.; 70 to 95° C.; 70 to 90° C.; 70 to 85° C.;70 to 80° C.; 70 to 75° C.; 75 to 200° C.; 75 to 190° C.; 75 to 180° C.;75 to 170° C.; 75 to 160° C.; 75 to 155° C.; 75 to 150° C.; 75 to 145°C.; 75 to 140° C.; 75 to 138° C.; 75 to 135° C.; 75 to 130° C.; 75 to125° C.; 75 to 120° C.; 75 to 115° C.; 75 to 110° C.; 75 to 105° C.; 75to 100° C.; 75 to 95° C.; 75 to 90° C.; 75 to 85° C.; 75 to 80° C.; 80to 200° C.; 80 to 190° C.; 80 to 180° C.; 80 to 170° C.; 80 to 160° C.;80 to 155° C.; 80 to 150° C.; 80 to 145° C.; 80 to 140° C.; 80 to 138°C.; 80 to 135° C.; 80 to 130° C.; 80 to 125° C.; 80 to 120° C.; 80 to115° C.; 80 to 110° C.; 80 to 105° C.; 80 to 100° C.; 80 to 95° C.; 80to 90° C.; 80 to 85° C.; 85 to 200° C.; 85 to 190° C.; 85 to 180° C.; 85to 170° C.; 85 to 160° C.; 85 to 155° C.; 85 to 150° C.; 85 to 145° C.;85 to 140° C.; 85 to 138° C.; 85 to 135° C.; 85 to 130° C.; 85 to 125°C.; 85 to 120° C.; 85 to 115° C.; 85 to 110° C.; 85 to 105° C.; 85 to100° C.; 85 to 95° C.; 85 to 90° C.; 90 to 200° C.; 90 to 190° C.; 90 to180° C.; 90 to 170° C.; 90 to 160° C.; 90 to 155° C.; 90 to 150° C.; 90to 145° C.; 90 to 140° C.; 90 to 138° C.; 90 to 135° C.; 90 to 130° C.;90 to 125° C.; 90 to 120° C.; 90 to 115° C.; 90 to 110° C.; 90 to 105°C.; 90 to 100° C.; 90 to 95° C.; 95 to 200° C.; 95 to 190° C.; 95 to180° C.; 95 to 170° C.; 95 to 160° C.; 95 to 155° C.; 95 to 150° C.; 95to 145° C.; 95 to 140° C.; 95 to 138° C.; 95 to 135° C.; 95 to 130° C.;95 to 125° C.; 95 to 120° C.; 95 to 115° C.; 95 to 110° C.; 95 to 105°C.; 95 to 100° C.; 100 to 200° C.; 100 to 190° C.; 100 to 180° C.; 100to 170° C.; 100 to 160° C.; 100 to 155° C.; 100 to 150° C.; 100 to 145°C.; 100 to 140° C.; 100 to 138° C.; 100 to 135° C.; 100 to 130° C.; 100to 125° C.; 100 to 120° C.; 100 to 115° C.; 100 to 110° C.; 105 to 200°C.; 105 to 190° C.; 105 to 180° C.; 105 to 170° C.; 105 to 160° C.; 105to 155° C.; 105 to 150° C.; 105 to 145° C.; 105 to 140° C.; 105 to 138°C.; 105 to 135° C.; 105 to 130° C.; 105 to 125° C.; 105 to 120° C.; 105to 115° C.; 105 to 110° C.; 110 to 200° C.; 110 to 190° C.; 110 to 180°C.; 110 to 170° C.; 110 to 160° C.; 110 to 155° C.; 110 to 150° C.; 110to 145° C.; 110 to 140° C.; 110 to 138° C.; 110 to 135° C.; 110 to 130°C.; 110 to 125° C.; 110 to 120° C.; 110 to 115° C.; 115 to 200° C.; 115to 190° C.; 115 to 180° C.; 115 to 170° C.; 115 to 160° C.; 115 to 155°C.; 115 to 150° C.; 115 to 145° C.; 115 to 140° C.; 115 to 138° C.; 115to 135° C.; 110 to 130° C.; 115 to 125° C.; 115 to 120° C.; 120 to 200°C.; 120 to 190° C.; 120 to 180° C.; 120 to 170° C.; 120 to 160° C.; 120to 155° C.; 120 to 150° C.; 120 to 145° C.; 120 to 140° C.; 120 to 138°C.; 120 to 135° C.; 120 to 130° C.; 125 to 200° C.; 125 to 190° C.; 125to 180° C.; 125 to 170° C.; 125 to 165° C.; 125 to 160° C.; 125 to 155°C.; 125 to 150° C.; 125 to 145° C.; 125 to 140° C.; 125 to 138° C.; 125to 135° C.; 127 to 200° C.; 127 to 190° C.; 127 to 180° C.; 127 to 170°C.; 127 to 160° C.; 127 to 150° C.; 127 to 145° C.; 127 to 140° C.; 127to 138° C.; 127 to 135° C.; 130 to 200° C.; 130 to 190° C.; 130 to 180°C.; 130 to 170° C.; 130 to 160° C.; 130 to 155° C.; 130 to 150° C.; 130to 145° C.; 130 to 140° C.; 130 to 138° C.; 130 to 135° C.; 135 to 200°C.; 135 to 190° C.; 135 to 180° C.; 135 to 170° C.; 135 to 160° C.; 135to 155° C.; 135 to 150° C.; 135 to 145° C.; 135 to 140° C.; 140 to 200°C.; 140 to 190° C.; 140 to 180° C.; 140 to 170° C.; 140 to 160° C.; 140to 155° C.; 140 to 150° C.; 140 to 145° C.; 148 to 200° C.; 148 to 190°C.; 148 to 180° C.; 148 to 170° C.; 148 to 160° C.; 148 to 155° C.; 148to 150° C.; greater than 148 to 200° C.; greater than 148 to 190° C.;greater than 148 to 180° C.; greater than 148 to 170° C.; greater than148 to 160° C.; greater than 148 to 155° C.; 150 to 200° C.; 150 to 190°C.; 150 to 180° C.; 150 to 170° C.; 150 to 160; 155 to 190° C.; 155 to180° C.; 155 to 170° C.; and 155 to 165° C.

In other aspects of the invention, the glycol component for thepolyesters useful in the containers of the invention include but are notlimited to at least one of the following combinations of ranges: 1 to 99mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 99 mole %1,4-cyclohexanedimethanol; 1 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 99 mole %1,4-cyclohexanedimethanol; 1 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 99 mole %1,4-cyclohexanedimethanol; 1 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 99 mole %1,4-cyclohexanedimethanol; 1 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 99 mole %1,4-cyclohexanedimethanol, 1 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 99 mole %1,4-cyclohexanedimethanol; 1 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 99 mole %1,4-cyclohexanedimethanol; 1 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 99 mole %1,4-cyclohexanedimethanol; 1 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 99 mole %1,4-cyclohexanedimethanol; 1 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 99 mole %1,4-cyclohexanedimethanol; 1 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 99 mole %1,4-cyclohexanedimethanol; 1 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 99 mole %1,4-cyclohexanedimethanol; 1 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 99 mole %1,4-cyclohexanedimethanol; 1 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 99 mole %1,4-cyclohexanedimethanol; 1 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 99 mole %1,4-cyclohexanedimethanol; 1 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 99 mole %1,4-cyclohexanedimethanol; 1 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 80 to 99 mole %1,4-cyclohexanedimethanol; 1 to 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 85 to 99 mole %1,4-cyclohexanedimethanol; 1 to 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 90 to 99 mole %1,4-cyclohexanedimethanol; and 1 to 5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 95 to 99 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the containers of the invention include but are notlimited to at least one of the following combinations of ranges: 0.01 to15 mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol and 85 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to less than 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 85 to 99.99mole % 1,4-cyclohexanedimethanol; 0.01 to 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 90 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to less than 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 90 to 99.99mole % 1,4-cyclohexanedimethanol; 0.01 to 9 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 91 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 8 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 92 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 7 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 93 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 95 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to less than 5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 95 to 99.99mole % 1,4-cyclohexanedimethanol; 0.01 to 4.5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 95.5 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 4 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 96 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 3.5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 96.5 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 3 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 97 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 2.5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 97.5 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 2 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 98 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 1.5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 98.5 to 99.99 mole %1,4-cyclohexanedimethanol; 0.01 to 1 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 99 to 99.99 mole %1,4-cyclohexanedimethanol; and 0.01 to 0.5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 99.5 to 99.99 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 3 to 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 90 to 97 mole %1,4-cyclohexanedimethanol; 3 to 9 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 91 to 97 mole %1,4-cyclohexanedimethanol; and 3 to 8 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 92 to 97 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 5 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 95 mole %1,4-cyclohexanedimethanol; 5 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 95 mole %1,4-cyclohexanedimethanol; 5 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 95 mole %1,4-cyclohexanedimethanol; 5 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 95 mole %1,4-cyclohexanedimethanol; 5 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 95 mole %1,4-cyclohexanedimethanol, 5 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 95 mole %1,4-cyclohexanedimethanol; 5 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 95 mole %1,4-cyclohexanedimethanol; 5 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 95 mole %1,4-cyclohexanedimethanol; 5 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 95 mole %1,4-cyclohexanedimethanol; 5 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 95 mole %1,4-cyclohexanedimethanol; and 5 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 95 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the containers of the invention include but are notlimited to at least one of the following combinations of ranges: 5 toless than 50 mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol and greaterthan 50 to 95 mole % 1,4-cyclohexanedimethanol; 5 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 95 mole %1,4-cyclohexanedimethanol; 5 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 95 mole %1,4-cyclohexanedimethanol; 5 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 95 mole %1,4-cyclohexanedimethanol; 5 to less than 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 65 to 95 mole %1,4-cyclohexanedimethanol; 5 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 95 mole %1,4-cyclohexanedimethanol; 5 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 95 mole %1,4-cyclohexanedimethanol; 5 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 80 to 95 mole %1,4-cyclohexanedimethanol; 5 to 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 85 to 95 mole %1,4-cyclohexanedimethanol; 5 to 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 90 to 95 mole %1,4-cyclohexanedimethanol; greater than 5 to less than 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and less than 90 to greater than95 mole % 1,4-cyclohexanedimethanol; 5.5 mole % to 9.5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 94.5 mole % to 90.5 mole %1,4-cyclohexanedimethanol; and 6 to 9 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 94 to 91 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 10 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 90 mole %1,4-cyclohexanedimethanol; 10 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 90 mole %1,4-cyclohexanedimethanol; 10 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 90 mole %1,4-cyclohexanedimethanol; 10 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 90 mole %1,4-cyclohexanedimethanol; 10 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 90 mole %1,4-cyclohexanedimethanol; 10 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 90 mole %1,4-cyclohexanedimethanol; 10 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 90 mole %1,4-cyclohexanedimethanol; 10 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 90 mole %1,4-cyclohexanedimethanol; 10 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 90 mole %1,4-cyclohexanedimethanol; 10 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 90 mole %1,4-cyclohexanedimethanol; 10 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 90 mole %1,4-cyclohexanedimethanol; 10 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 90 mole %1,4-cyclohexanedimethanol; 10 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 90 mole %1,4-cyclohexanedimethanol; 10 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 90 mole %1,4-cyclohexanedimethanol; 10 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 90 mole %1,4-cyclohexanedimethanol; 10 to less than 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 65 to 90%1,4-cyclohexanedimethanol; 10 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 90 mole %1,4-cyclohexanedimethanol; 10 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 90 mole %1,4-cyclohexanedimethanol; 10 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 80 to 90 mole %1,4-cyclohexanedimethanol; and 10 to 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 85 to 90 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: greater than 10 to 99mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to less than 90mole % 1,4-cyclohexanedimethanol; greater than 10 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to less than90 mole % 1,4-cyclohexanedimethanol; greater than 10 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to less than 90 mole %1,4-cyclohexanedimethanol; 10 to less than 34 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 66 to 90%1,4-cyclohexanedimethanol; greater than 10 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to less than 90 mole %1,4-cyclohexanedimethanol; greater than 10 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 80 to less than 90 mole %1,4-cyclohexanedimethanol; and greater than 10 to 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 85 to less than 90 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 11 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 89 mole %1,4-cyclohexanedimethanol; 11 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 89 mole %1,4-cyclohexanedimethanol; 11 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 89 mole %1,4-cyclohexanedimethanol; 11 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 89 mole %1,4-cyclohexanedimethanol; 11 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 89 mole %1,4-cyclohexanedimethanol; 11 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 89 mole %1,4-cyclohexanedimethanol; 11 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 89 mole %1,4-cyclohexanedimethanol; 11 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 89 mole %1,4-cyclohexanedimethanol; 11 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 89 mole %1,4-cyclohexanedimethanol; 11 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 89 mole %1,4-cyclohexanedimethanol; 11 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 89 mole %1,4-cyclohexanedimethanol; 11 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 89 mole %1,4-cyclohexanedimethanol; 11 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 89 mole %1,4-cyclohexanedimethanol; 11 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 89 mole %1,4-cyclohexanedimethanol; 11 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 89 mole %1,4-cyclohexanedimethanol; 11 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 89 mole %1,4-cyclohexanedimethanol; 11 to 24 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 76 to 89 mole %1,4-cyclohexanedimethanol; and 11 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 89 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 12 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 88 mole %1,4-cyclohexanedimethanol; 12 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 88 mole %1,4-cyclohexanedimethanol; 12 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 88 mole %1,4-cyclohexanedimethanol; 12 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 88 mole %1,4-cyclohexanedimethanol; 12 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 88 mole %1,4-cyclohexanedimethanol; 12 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 88 mole %1,4-cyclohexanedimethanol; 12 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 88 mole %1,4-cyclohexanedimethanol; 12 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 88 mole %1,4-cyclohexanedimethanol; 12 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 88 mole %1,4-cyclohexanedimethanol; 12 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 88 mole %1,4-cyclohexanedimethanol; 12 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 88 mole %1,4-cyclohexanedimethanol; 12 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 88 mole %1,4-cyclohexanedimethanol; 12 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 88 mole %1,4-cyclohexanedimethanol; 12 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 88 mole %1,4-cyclohexanedimethanol; 12 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 88 mole %1,4-cyclohexanedimethanol; 12 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 88 mole %1,4-cyclohexanedimethanol; 12 to 24 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 76 to 88 mole %1,4-cyclohexanedimethanol; and 12 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 88 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 13 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 87 mole %1,4-cyclohexanedimethanol; 13 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 87 mole %1,4-cyclohexanedimethanol; 13 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 87 mole %1,4-cyclohexanedimethanol; 13 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 87 mole %1,4-cyclohexanedimethanol; 13 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 87 mole %1,4-cyclohexanedimethanol; 13 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 87 mole %1,4-cyclohexanedimethanol; 13 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 87 mole %1,4-cyclohexanedimethanol; 13 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 87 mole %1,4-cyclohexanedimethanol; 13 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 87 mole %1,4-cyclohexanedimethanol; 13 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 87 mole %1,4-cyclohexanedimethanol; 13 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 87 mole %1,4-cyclohexanedimethanol; 13 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 87 mole %1,4-cyclohexanedimethanol; 13 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 87 mole %1,4-cyclohexanedimethanol; 13 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 87 mole %1,4-cyclohexanedimethanol; 13 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 87 mole %1,4-cyclohexanedimethanol; 13 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 87 mole %1,4-cyclohexanedimethanol; 13 to 24 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 76 to 87 mole %1,4-cyclohexanedimethanol; and 13 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 87 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 14 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 86 mole %1,4-cyclohexanedimethanol; 14 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 86 mole %1,4-cyclohexanedimethanol; 14 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 86 mole %1,4-cyclohexanedimethanol; 14 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 86 mole %1,4-cyclohexanedimethanol; 14 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 86 mole %1,4-cyclohexanedimethanol; 14 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 86 mole %1,4-cyclohexanedimethanol; 14 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 86 mole %1,4-cyclohexanedimethanol; 14 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 86 mole %1,4-cyclohexanedimethanol; 14 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 86 mole %1,4-cyclohexanedimethanol; 14 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 86 mole %1,4-cyclohexanedimethanol; 14 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 86 mole %1,4-cyclohexanedimethanol; 14 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 86 mole %1,4-cyclohexanedimethanol; 14 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 86 mole %1,4-cyclohexanedimethanol; 14 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 86 mole %1,4-cyclohexanedimethanol; 14 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 86 mole %1,4-cyclohexanedimethanol; 14 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 86 mole %1,4-cyclohexanedimethanol; 14 to 24 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 76 to 86 mole %1,4-cyclohexanedimethanol; and 14 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 86 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 15 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 85 mole %1,4-cyclohexanedimethanol; 15 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 85 mole %1,4-cyclohexanedimethanol; 15 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 85 mole %1,4-cyclohexanedimethanol; 15 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 85 mole %1,4-cyclohexanedimethanol; 15 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 85 mole %1,4-cyclohexanedimethanol; 15 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 85 mole %1,4-cyclohexanedimethanol; 15 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 85 mole %1,4-cyclohexanedimethanol; 15 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 85 mole %1,4-cyclohexanedimethanol; 15 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 85 mole %1,4-cyclohexanedimethanol; 15 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 85 mole %1,4-cyclohexanedimethanol; 15 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 85 mole %1,4-cyclohexanedimethanol; 15 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 85 mole %1,4-cyclohexanedimethanol; 15 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 85 mole %1,4-cyclohexanedimethanol; 15 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 85 mole %1,4-cyclohexanedimethanol; 15 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 85 mole %1,4-cyclohexanedimethanol; 15 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 85 mole %1,4-cyclohexanedimethanol; 15 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 85 mole %1,4-cyclohexanedimethanol; and 15 to 24 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 76 to 85 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 20 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 80 mole %1,4-cyclohexanedimethanol; 20 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 80 mole %1,4-cyclohexanedimethanol; 20 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 80 mole %1,4-cyclohexanedimethanol; 20 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 80 mole %1,4-cyclohexanedimethanol; 20 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 80 mole %1,4-cyclohexanedimethanol; 20 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 80 mole %1,4-cyclohexanedimethanol; 20 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 80 mole %1,4-cyclohexanedimethanol; 20 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 80 mole %1,4-cyclohexanedimethanol; 20 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 80 mole %1,4-cyclohexanedimethanol; 20 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 80 mole %1,4-cyclohexanedimethanol; 20 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 80 mole %1,4-cyclohexanedimethanol; 20 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 80 mole %1,4-cyclohexanedimethanol; 20 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 80 mole %1,4-cyclohexanedimethanol; 20 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 80 mole %1,4-cyclohexanedimethanol; 20 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 80 mole %1,4-cyclohexanedimethanol; 20 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 80 mole %1,4-cyclohexanedimethanol; and 20 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 75 to 80 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 25 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 75 mole %1,4-cyclohexanedimethanol; 25 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 75 mole %1,4-cyclohexanedimethanol; 25 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 75 mole %1,4-cyclohexanedimethanol; 25 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 75 mole %1,4-cyclohexanedimethanol; 25 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 75 mole %1,4-cyclohexanedimethanol; 25 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 75 mole %1,4-cyclohexanedimethanol; 25 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 75 mole %1,4-cyclohexanedimethanol; 25 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 75 mole %1,4-cyclohexanedimethanol; 25 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 75 mole %1,4-cyclohexanedimethanol; 25 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 75 mole %1,4-cyclohexanedimethanol; 25 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 75 mole %1,4-cyclohexanedimethanol; 25 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 75 mole %1,4-cyclohexanedimethanol; 25 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 75 mole %1,4-cyclohexanedimethanol; 25 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 75 mole %1,4-cyclohexanedimethanol; 25 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 75 mole %1,4-cyclohexanedimethanol; and 25 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 70 to 75 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 30 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 70 mole %1,4-cyclohexanedimethanol; 30 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 70 mole %1,4-cyclohexanedimethanol; 30 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 70 mole %1,4-cyclohexanedimethanol; 30 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 70 mole %1,4-cyclohexanedimethanol; 30 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 70 mole %1,4-cyclohexanedimethanol; 30 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 70 mole %1,4-cyclohexanedimethanol; 30 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 70 mole %1,4-cyclohexanedimethanol; 30 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 70 mole %1,4-cyclohexanedimethanol; 30 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 70 mole %1,4-cyclohexanedimethanol; 30 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 70 mole %1,4-cyclohexanedimethanol; 30 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 70 mole %1,4-cyclohexanedimethanol; 30 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 70 mole %1,4-cyclohexanedimethanol; 30 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 70 mole %1,4-cyclohexanedimethanol; 30 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 70 mole %1,4-cyclohexanedimethanol; 30 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 70 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 35 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 65 mole %1,4-cyclohexanedimethanol; 35 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 65 mole %1,4-cyclohexanedimethanol; 35 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 65 mole %1,4-cyclohexanedimethanol; 35 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 65 mole %1,4-cyclohexanedimethanol; 35 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 65 mole %1,4-cyclohexanedimethanol; 35 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 65 mole %1,4-cyclohexanedimethanol; 35 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 65 mole %1,4-cyclohexanedimethanol; 35 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 65 mole %1,4-cyclohexanedimethanol; 35 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 65 mole %1,4-cyclohexanedimethanol; 35 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 65 mole %1,4-cyclohexanedimethanol; 35 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 65 mole %1,4-cyclohexanedimethanol; 35 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 65 mole %1,4-cyclohexanedimethanol; 35 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 65 mole %1,4-cyclohexanedimethanol; 35 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 65 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 40 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 60 mole %1,4-cyclohexanedimethanol; 40 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 60 mole %1,4-cyclohexanedimethanol; 40 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 60 mole %1,4-cyclohexanedimethanol; 40 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 60 mole %1,4-cyclohexanedimethanol; 40 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 60 mole %1,4-cyclohexanedimethanol; 40 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 60 mole %1,4-cyclohexanedimethanol; 40 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 60 mole %1,4-cyclohexanedimethanol; 40 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 60 mole %1,4-cyclohexanedimethanol; 40 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 60 mole %1,4-cyclohexanedimethanol; 40 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 60 mole %1,4-cyclohexanedimethanol; 40 to less than 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 50 to 60 mole %1,4-cyclohexanedimethanol; 40 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 60 mole %1,4-cyclohexanedimethanol; and 40 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 55 to 60 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 45 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 55 mole %1,4-cyclohexanedimethanol; 45 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 55 mole %1,4-cyclohexanedimethanol; 45 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 55 mole %1,4-cyclohexanedimethanol; 45 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 55 mole %1,4-cyclohexanedimethanol; 45 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 55 mole %1,4-cyclohexanedimethanol; 45 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 55 mole %1,4-cyclohexanedimethanol; 45 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 55 mole %1,4-cyclohexanedimethanol; 45 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 55 mole %1,4-cyclohexanedimethanol; 45 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 55 mole %1,4-cyclohexanedimethanol; greater than 45 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to less than 55 mole %1,4-cyclohexanedimethanol; 45 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 55 mole %1,4-cyclohexanedimethanol; and 45 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 50 to 60 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: greater than 50 to 99mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to less than 50mole % 1,4-cyclohexanedimethanol; greater than 50 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to less than 50 mole %1,4-cyclohexanedimethanol; greater than 50 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to less than 50 mole %1,4-cyclohexanedimethanol; greater than 50 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to less than 50 mole %1,4-cyclohexanedimethanol; greater than 50 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to less than 50 mole %1,4-cyclohexanedimethanol; greater than 50 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to less than 50 mole %1,4-cyclohexanedimethanol; greater than 50 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to less than 50 mole %1,4-cyclohexanedimethanol; greater than 50 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to less than 50 mole %1,4-cyclohexanedimethanol; greater than 50 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to less than 50 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 55 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 45 mole %1,4-cyclohexanedimethanol; 55 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 45 mole %1,4-cyclohexanedimethanol; 55 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 45 mole %1,4-cyclohexanedimethanol; 55 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 45 mole %1,4-cyclohexanedimethanol; 55 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 45 mole %1,4-cyclohexanedimethanol; 55 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 45 mole %1,4-cyclohexanedimethanol; 55 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 45 mole %1,4-cyclohexanedimethanol; 55 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 45 mole %1,4-cyclohexanedimethanol; and 55 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 40 to 45 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 60 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 40 mole %1,4-cyclohexanedimethanol; 60 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 40 mole %1,4-cyclohexanedimethanol; 60 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 40 mole %1,4-cyclohexanedimethanol; 60 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 40 mole %1,4-cyclohexanedimethanol; 60 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 40 mole %1,4-cyclohexanedimethanol; 60 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 40 mole %1,4-cyclohexanedimethanol; and 60 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 40 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 65 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 35 mole %1,4-cyclohexanedimethanol; 65 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 35 mole %1,4-cyclohexanedimethanol; 65 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 35 mole %1,4-cyclohexanedimethanol; 65 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 35 mole %1,4-cyclohexanedimethanol; 65 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 35 mole %1,4-cyclohexanedimethanol; 65 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 35 mole %1,4-cyclohexanedimethanol; and 65 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 30 to 35 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 70 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 30 mole %1,4-cyclohexanedimethanol; 70 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 30 mole %1,4-cyclohexanedimethanol; 70 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 30 mole %1,4-cyclohexanedimethanol; 70 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 30 mole %1,4-cyclohexanedimethanol; 70 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 30 mole %1,4-cyclohexanedimethanol; 70 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 25 to 30 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 75 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 25 mole %1,4-cyclohexanedimethanol; 75 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 25 mole %1,4-cyclohexanedimethanol; 75 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 25 mole %1,4-cyclohexanedimethanol; and 75 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 15 to 25 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges: 80 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 20 mole %1,4-cyclohexanedimethanol; 80 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 5 to 20 mole %1,4-cyclohexanedimethanol; 80 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 10 to 20 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following combinations of ranges 37 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 20 to 63 mole %1,4-cyclohexanedimethanol; 40 to less than 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and greater than 55 to 60 mole %1,4-cyclohexanedimethanol; greater than 45 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to less than 55 mole %1,4-cyclohexanedimethanol; and 46 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 45 to 54 mole %1,4-cyclohexanedimethanol; and 46 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 35 to 54 mole %1,4-cyclohexanedimethanol.

In other aspects of the invention where the mole percent of2,2,4,4-tetramethyl-1,3-cyclobutanediol is present at 0.01 to less than5 mole % based on the mole percentages for the diol component equaling100 mole % and where the presence of CHDM is optional, the glycolcomponent for the polyesters useful the invention include but are notlimited to at least of the following combinations of ranges: 0.01 toless than 5 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues,greater than 0.01 to 95 mole % of ethylene glycol residues, and 0 to99.98 mole % of 1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to94.99 mole % of ethylene glycol residues, and 0.01 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to90 mole % of ethylene glycol residues, and 5 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to85 mole % of ethylene glycol residues, and 10 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to80 mole % of ethylene glycol residues, and 15 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to75 mole % of ethylene glycol residues, and 20 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to70 mole % of ethylene glycol residues, and 25 to 99.98 mole % of1,4-cyclohexanedimethanol; greater than 0.01 to 65 mole % of ethyleneglycol residues, and 30 to 99.98 mole % of 1,4-cyclohexanedimethanol;0.01 to less than 5 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediolresidues, greater than 0.01 to 60 mole % of ethylene glycol residues,and 35 to 99.98 mole % of 1,4-cyclohexanedimethanol; 0.01 to less than 5mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than0.01 to 55 mole % of ethylene glycol residues, and 40 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to50 mole % of ethylene glycol residues, and 45 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to45 mole % of ethylene glycol residues, and 50 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to40 mole % of ethylene glycol residues, and 55 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to35 mole % of ethylene glycol residues, and 60 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to30 mole % of ethylene glycol residues, and 65 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to25 mole % of ethylene glycol residues, and 70 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to20 mole % of ethylene glycol residues, and 75 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to15 mole % of ethylene glycol residues, and 80 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to10 mole % of ethylene glycol residues, and 85 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, greater than 0.01 to 5mole % of ethylene glycol residues, and 90 to 99.98 mole % of1,4-cyclohexanedimethanol; 0.01 to less than 5 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, and greater than 0.01to 5 mole % of ethylene glycol residues, and 90 to 99.98 mole % of1,4-cyclohexanedimethanol.

The glycol component may also contain one of the following ranges of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues: 0.01 to 4.5 mole %;0.01 to 4 mole %; 0.01 to 3.5 mole %; 0.01 to 3 mole %; 0.01 to 2.5 mole%; 0.01 to 2.0 mole %; 0.01 to 2.5 mole %; 0.01 to 2 mole %; 0.01 to 1.5mole %; 0.01 to 1.0 mole %; and 0.01 to 0.5 mole %. The remainder of theglycol component can be any amount of 1,4-cyclohexanedimethanol and/orethylene glycol so long as the total amount of the glycol componentequals 100 mole %.

In addition to the diols set forth above, the polyesters useful in thepolyester compositions of the containers of the invention may be madefrom 1,3-propanediol, 1,4-butanediol, or mixtures thereof. It iscontemplated that compositions of the invention made from1,3-propanediol, 1,4-butanediol, or mixtures thereof can possess atleast one of the Tg ranges described herein, at least one of theinherent viscosity ranges described herein, and/or at least one of theglycol or diacid ranges described herein. In addition or in thealternative, the polyesters made from 1,3-propanediol or 1,4-butanediolor mixtures thereof may also be made from 1,4-cyclohexanedmethanol in atleast one of the following amounts: from 0.1 to 99 mole %; 0.1 to 90mole %; from 0.1 to 80 mole %; from 0.1 to 70 mole %; from 0.1 to 60mole %; from 0.1 to 50 mole %; from 0.1 to 40 mole %; from 0.1 to 35mole %; from 0.1 to 30 mole %; from 0.1 to 25 mole %; from 0.1 to 20mole %; from 0.1 to 15 mole %; from 0.1 to 10 mole %; from 0.1 to 5 mole%; from 1 to 99 mole %; from 1 to 90 mole %; from 1 to 80 mole %; from 1to 70 mole %; from 1 to 60 mole %; from 1 to 50 mole %; from 1 to 40mole %; from 1 to 35 mole %; from 1 to 30 mole %; from 1 to 25 mole %;from 1 to 20 mole %; from 1 to 15 mole %; from 1 to 10 mole %; from 1 to5 mole %; from 5 to 80 mole %; 5 to 70 mole %; from 5 to 60 mole %; from5 to 50 mole %; from 5 to 40 mole %; from 5 to 35 mole %; from 5 to 30mole %; from 5 to 25 mole %; from 5 to 20 mole %; and from 5 to 15 mole%; from 5 to 10 mole %; from 10 to 99 mole %; from 10 to 90 mole %; from10 to 80 mole %; from 10 to 70 mole %; from 10 to 60 mole %; from 10 to50 mole %; from 10 to 40 mole %; from 10 to 35 mole %; from 10 to 30mole %; from 10 to 25 mole %; from 10 to 20 mole %; from 10 to 15 mole%; from 20 to 99 mole %; 20 to 95 mole %; from 20 to 80 mole %; from 20to 70 mole %; from 20 to 60 mole %; from 20 to 50 mole %; from 20 to 40mole %; from 20 to 35 mole %; from 20 to 30 mole %; and from 20 to 25mole %.

For embodiments of the invention, the polyesters useful in the inventionmay exhibit at least one of the following inherent viscosities asdetermined in 60/40 (wt/wt) phenol/tetrachloroethane at a concentrationof 0.5 g/100 ml at 25° C., 0.10 to 1.2 dL/g; 0.10 to 1.1 dL/g; 0.10 to 1dL/g; 0.10 to less than 1 dL/g; 0.10 to 0.98 dL/g; 0.10 to 0.95 dL/g;0.10 to 0.90 dL/g; 0.10 to 0.85 dL/g; 0.10 to 0.80 dL/g; 0.10 to 0.75dL/g; 0.10 to less than 0.75 dL/g; 0.10 to 0.72 dL/g; 0.10 to 0.70 dL/g;0.10 to less than 0.70 dL/g; 0.10 to 0.68 dL/g; 0.10 to less than 0.68dL/g; 0.10 to 0.65 dL/g; 0.10 to 0.6 dL/g; 0.10 to 0.55 dL/g; 0.10 to0.5 dL/g; 0.10 to 0.4 dL/g; 0.10 to 0.35 dL/g; 0.20 to 1.2 dL/g; 0.20 to1.1 dL/g; 0.20 to 1 dL/g; 0.20 to less than 1 dL/g; 0.20 to 0.98 dL/g;0.20 to 0.95 dL/g; 0.20 to 0.90 dL/g; 0.20 to 0.85 dL/g; 0.20 to 0.80dL/g; 0.20 to 0.75 dL/g; 0.20 to less than 0.75 dL/g; 0.20 to 0.72 dL/g;0.20 to 0.70 dL/g; 0.20 to less than 0.70 dL/g; 0.20 to 0.68 dL/g; 0.20to less than 0.68 dL/g; 0.20 to 0.65 dL/g; 0.20 to 0.6 dL/g; 0.20 to0.55 dL/g; 0.20 to 0.5 dL/g; 0.20 to 0.4 dL/g; 0.20 to 0.35 dL/g; 0.35to 1.2 dL/g; 0.35 to 1.1 dL/g; 0.35 to 1 dL/g; 0.35 to less than 1 dL/g;0.35 to 0.98 dL/g; 0.35 to 0.95 dL/g; 0.35 to 0.90 dL/g; 0.35 to 0.85dL/g; 0.35 to 0.80 dL/g; 0.35 to 0.75 dL/g; 0.35 to less than 0.75 dL/g;0.35 to 0.72 dL/g; 0.35 to 0.70 dL/g; 0.35 to less than 0.70 dL/g; 0.35to 0.68 dL/g; 0.35 to less than 0.68 dL/g; 0.35 to 0.65 dL/g; 0.40 to1.2 dL/g; 0.40 to 1.1 dL/g; 0.40 to 1 dL/g; 0.40 to less than 1 dL/g;0.40 to 0.98 dL/g; 0.40 to 0.95 dL/g; 0.40 to 0.90 dL/g; 0.40 to 0.85dL/g; 0.40 to 0.80 dL/g; 0.40 to 0.75 dL/g; 0.40 to less than 0.75 dL/g;0.40 to 0.72 dL/g; 0.40 to 0.70 dL/g; 0.40 to less than 0.70 dL/g; 0.40to 0.68 dL/g; 0.40 to less than 0.68 dL/g; 0.40 to 0.65 dL/g; greaterthan 0.42 to 1.2 dL/g; greater than 0.42 to 1.1 dL/g; greater than 0.42to 1 dL/g; greater than 0.42 to less than 1 dL/g; greater than 0.42 to0.98 dL/g; greater than 0.42 to 0.95 dL/g; greater than 0.42 to 0.90dL/g; greater than 0.42 to 0.85 dL/g; greater than 0.42 to 0.80 dL/g;greater than 0.42 to 0.75 dL/g; greater than 0.42 to less than 0.75dL/g; greater than 0.42 to 0.72 dL/g; greater than 0.42 to 0.70 dL/g;greater than 0.42 to less than 0.70 dL/g; greater than 0.42 to 0.68dL/g; greater than 0.42 to less than 0.68 dL/g; and greater than 0.42 to0.65 dL/g.

For embodiments of the invention, the polyesters useful in the inventionmay exhibit at least one of the following inherent viscosities asdetermined in 60/40 (wt/wt) phenol/tetrachloroethane at a concentrationof 0.5 g/100 ml at 25° C., 0.45 to 1.2 dL/g; 0.45 to 1.1 dL/g; 0.45 to 1dL/g; 0.45 to 0.98 dL/g; 0.45 to 0.95 dL/g; 0.45 to 0.90 dL/g; 0.45 to0.85 dL/g; 0.45 to 0.80 dL/g; 0.45 to 0.75 dL/g; 0.45 to less than 0.75dL/g; 0.45 to 0.72 dL/g; 0.45 to 0.70 dL/g; 0.45 to less than 0.70 dL/g;0.45 to 0.68 dL/g; 0.45 to less than 0.68 dL/g; 0.45 to 0.65 dL/g; 0.50to 1.2 dL/g; 0.50 to 1.1 dL/g; 0.50 to 1 dL/g; 0.50 to less than 1 dL/g;0.50 to 0.98 dL/g; 0.50 to 0.95 dL/g; 0.50 to 0.90 dL/g; 0.50 to 0.85dL/g; 0.50 to 0.80 dL/g; 0.50 to 0.75 dL/g; 0.50 to less than 0.75 dL/g;0.50 to 0.72 dL/g; 0.50 to 0.70 dL/g; 0.50 to less than 0.70 dL/g; 0.50to 0.68 dL/g; 0.50 to less than 0.68 dL/g; 0.50 to 0.65 dL/g; 0.55 to1.2 dL/g; 0.55 to 1.1 dL/g; 0.55 to 1 dL/g; 0.55 to less than 1 dL/g;0.55 to 0.98 dL/g; 0.55 to 0.95 dL/g; 0.55 to 0.90 dL/g; 0.55 to 0.85dL/g; 0.55 to 0.80 dL/g; 0.55 to 0.75 dL/g; 0.55 to less than 0.75 dL/g;0.55 to 0.72 dL/g; 0.55 to 0.70 dL/g; 0.55 to less than 0.70 dL/g; 0.55to 0.68 dL/g; 0.55 to less than 0.68 dL/g; 0.55 to 0.65 dL/g; 0.58 to1.2 dL/g; 0.58 to 1.1 dL/g; 0.58 to 1 dL/g; 0.58 to less than 1 dL/g;0.58 to 0.98 dL/g; 0.58 to 0.95 dL/g; 0.58 to 0.90 dL/g; 0.58 to 0.85dL/g; 0.58 to 0.80 dL/g; 0.58 to 0.75 dL/g; 0.58 to less than 0.75 dL/g;0.58 to 0.72 dL/g; 0.58 to 0.70 dL/g; 0.58 to less than 0.70 dL/g; 0.58to 0.68 dL/g; 0.58 to less than 0.68 dL/g; 0.58 to 0.65 dL/g; 0.60 to1.2 dL/g; 0.60 to 1.1 dL/g; 0.60 to 1 dL/g; 0.60 to less than 1 dL/g;0.60 to 0.98 dL/g; 0.60 to 0.95 dL/g; 0.60 to 0.90 dL/g; 0.60 to 0.85dL/g; 0.60 to 0.80 dL/g; 0.60 to 0.75 dL/g; 0.60 to less than 0.75 dL/g;0.60 to 0.72 dL/g; 0.60 to 0.70 dL/g; 0.60 to less than 0.70 dL/g; 0.60to 0.68 dL/g; 0.60 to less than 0.68 dL/g; 0.60 to 0.65 dL/g; 0.65 to1.2 dL/g; 0.65 to 1.1 dL/g; 0.65 to 1 dL/g; 0.65 to less than 1 dL/g;0.65 to 0.98 dL/g; 0.65 to 0.95 dL/g; 0.65 to 0.90 dL/g; 0.65 to 0.85dL/g; 0.65 to 0.80 dL/g; 0.65 to 0.75 dL/g; 0.65 to less than 0.75 dL/g;0.65 to 0.72 dL/g; 0.65 to 0.70 dL/g; 0.65 to less than 0.70 dL/g; 0.68to 1.2 dL/g; 0.68 to 1.1 dL/g; 0.68 to 1 dL/g; 0.68 to less than 1 dL/g;0.68 to 0.98 dL/g; 0.68 to 0.95 dL/g; 0.68 to 0.90 dL/g; 0.68 to 0.85dL/g; 0.68 to 0.80 dL/g; 0.68 to 0.75 dL/g; 0.68 to less than 0.75 dL/g;0.68 to 0.72 dL/g; greater than 0.76 dL/g to 1.2 dL/g; greater than 0.76dL/g to 1.1 dL/g; greater than 0.76 dL/g to 1 dL/g; greater than 0.76dL/g to less than 1 dL/g; greater than 0.76 dL/g to 0.98 dL/g; greaterthan 0.76 dL/g to 0.95 dL/g; greater than 0.76 dL/g to 0.90 dL/g;greater than 0.80 dL/g to 1.2 dL/g; greater than 0.80 dL/g to 1.1 dL/g;greater than 0.80 dL/g to 1 dL/g; greater than 0.80 dL/g to less than 1dL/g; greater than 0.80 dL/g to 1.2 dL/g; greater than 0.80 dL/g to 0.98dL/g; greater than 0.80 dL/g to 0.95 dL/g; greater than 0.80 dL/g to0.90 dL/g.

For the desired polyester, the molar ratio of cis/trans2,2,4,4-tetramethyl-1,3-cyclobutanediol can vary from the pure form ofeach or mixtures thereof. In certain embodiments, the molar percentagesfor cis and/or trans 2,2,4,4-tetramethyl-1,3-cyclobutanediol are greaterthan 50 mole % cis and less than 50 mole % trans; or greater than 55mole % cis and less than 45 mole % trans; or 30 to 70 mole % cis and 70to 30 mole % trans; or 40 to 60 mole % cis and 60 to 40 mole % trans; or50 to 70 mole % trans and 50 to 30% cis; or 50 to 70 mole % cis and 50to 30% trans; or 60 to 70 mole % cis and 30 to 40 mole % trans; orgreater than 70 mole % cis and less than 30 mole % trans; wherein thetotal sum of the mole percentages for cis- andtrans-2,2,4,4-tetramethyl-1,3-cyclobutanediol is equal to 100 mole %.The molar ratio of cis/trans 1,4-cyclohexandimethanol can vary withinthe range of 50/50 to 0/100, for example, between 40/60 to 20/80.

It is contemplated that compositions useful in the container(s) of theinvention can possess at least one of the inherent viscosity rangesdescribed herein and at least one of the monomer ranges for thecompositions described herein unless otherwise stated. It is alsocontemplated that compositions useful in the container(s) of theinvention can possess at least one of the Tg ranges described herein andat least one of the monomer ranges for the compositions described hereinunless otherwise stated. It is also contemplated that compositionsuseful in the container(s) of the invention can possess at least one ofthe inherent viscosity ranges described herein, at least one of the Tgranges described herein, and at least one of the monomer ranges for thecompositions described herein unless otherwise stated.

In certain embodiments, terephthalic acid or an ester thereof, such as,for example, dimethyl terephthalate or a mixture of terephthalic acidresidues and an ester thereof can make up a portion or all of thedicarboxylic acid component used to form the polyesters useful in theinvention. In certain embodiments, terephthalic acid residues can makeup a portion or all of the dicarboxylic acid component used to form thepresent polyester at a concentration of at least 70 mole %, such as atleast 80 mole %, at least 90 mole % at least 95 mole %, at least 99 mole%, or even 100 mole %. In certain embodiments, higher amounts ofterephthalic acid can be used in order to produce a higher impactstrength polyester. For purposes of this disclosure, the terms“terephthalic acid” and “dimethyl terephthalate” are usedinterchangeably herein. In one embodiment, dimethyl terephthalate ispart or all of the dicarboxylic acid component used to make thepolyesters useful in the present invention. For the purposes of thisdisclosure, the terms: “terephthalic acid” and “dimethyl terephthalate”are used interchangeably herein. In all embodiments, ranges of from 70to 100 mole %; or 80 to 100 mole %; or 90 to 100 mole %; or 99 to 100mole %; or 100 mole % terephthalic acid and/or dimethyl terephthalateand/or mixtures thereof may be used.

In addition to terephthalic acid, the dicarboxylic acid component of thepolyester useful in the invention can comprise up to 30 mole %, up to 20mole %, up to 10 mole %, up to 5 mole %, or up to 1 mole % of one ormore modifying aromatic dicarboxylic acids. Yet another embodimentcontains 0 mole % modifying aromatic dicarboxylic acids. Thus, ifpresent, it is contemplated that the amount of one or more modifyingaromatic dicarboxylic acids can range from any of these precedingendpoint values including, for example, from 0.01 to 30 mole %, 0.01 to20 mole %, from 0.01 to 10 mole %, from 0.01 to 5 mole % and from 0.01to 1 mole. In one embodiment, modifying aromatic dicarboxylic acids thatmay be used in the present invention include but are not limited tothose having up to 20 carbon atoms, and which can be linear,para-oriented, or symmetrical. Examples of modifying aromaticdicarboxylic acids which may be used in this invention include, but arenot limited to, isophthalic acid, 4,4′-biphenyldicarboxylic acid, 1,4-,1,5-, 2,6-, 2,7-naphthalenedicarboxylic acid, andtrans-4,4′-stilbenedicarboxylic acid, and esters thereof. In oneembodiment, the modifying aromatic dicarboxylic acid is isophthalicacid.

The carboxylic acid component of the polyesters useful in the inventioncan be further modified with up to 10 mole %, such as up to 5 mole % orup to 1 mole % of one or more aliphatic dicarboxylic acids containing2-16 carbon atoms, such as, for example, malonic, succinic, glutaric,adipic, pimelic, suberic, azelaic and dodecanedioic dicarboxylic acids.Certain embodiments can also comprise 0.01 or more mole %, such as 0.1or more mole %, 1 or more mole %, 5 or more mole %, or 10 or more mole %of one or more modifying aliphatic dicarboxylic acids. Yet anotherembodiment contains 0 mole % modifying aliphatic dicarboxylic acids.Thus, if present, it is contemplated that the amount of one or moremodifying aliphatic dicarboxylic acids can range from any of thesepreceding endpoint values including, for example, from 0.01 to 10 mole %and from 0.1 to 10 mole %. The total mole % of the dicarboxylic acidcomponent is 100 mole %.

Esters of terephthalic acid and the other modifying dicarboxylic acidsor their corresponding esters and/or salts may be used instead of thedicarboxylic acids. Suitable examples of dicarboxylic acid estersinclude, but are not limited to, the dimethyl, diethyl, dipropyl,diisopropyl, dibutyl, and diphenyl esters. In one embodiment, the estersare chosen from at least one of the following: methyl, ethyl, propyl,isopropyl, and phenyl esters.

The 1,4-cyclohexanedimethanol may be cis, trans, or a mixture thereof,for example, a cis/trans ratio of 60:40 to 40:60. In another embodiment,the trans-1,4-cyclohexanedimethanol can be present in an amount of 60 to80 mole %.

The glycol component of the polyester portion of the polyestercomposition useful in the invention can contain 25 mole % or less of oneor more modifying glycols which are not2,2,4,4-tetramethyl-1,3-cyclobutanediol or 1,4-cyclohexanedimethanol; inone embodiment, the polyesters useful in the invention may contain lessthan 15 mole % or of one or more modifying glycols. In anotherembodiment, the polyesters useful in the invention can contain 10 mole %or less of one or more modifying glycols. In another embodiment, thepolyesters useful in the invention can contain 5 mole % or less of oneor more modifying glycols. In another embodiment, the polyesters usefulin the invention can contain 3 mole % or less of one or more modifyingglycols. In another embodiment, the polyesters useful in the inventioncan contain 0 mole % modifying glycols. Certain embodiments can alsocontain 0.01 or more mole %, such as 0.1 or more mole %, 1 or more mole%, 5 or more mole %, or 10 or more mole % of one or more modifyingglycols. Thus, if present, it is contemplated that the amount of one ormore modifying glycols can range from any of these preceding endpointvalues including, for example, from 0.01 to 15 mole % and from 0.1 to 10mole %.

Modifying glycols useful in the polyesters useful in the invention referto diols other than 2,2,4,4-tetramethyl-1,3-cyclobutanediol and1,4-cyclohexanedimethanol and can contain 2 to 16 carbon atoms. Examplesof suitable modifying glycols include, but are not limited to, ethyleneglycol, 1,2-propanediol, 1,3-propanediol, neopentyl glycol,1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, p-xylene glycol, ormixtures thereof. In one embodiment, the modifying glycol is ethyleneglycol. In another embodiment, the modifying glycols include, but arenot limited to, 1,3-propanediol and 1,4-butanediol. In anotherembodiment, ethylene glycol is excluded as a modifying diol. In anotherembodiment, 1,3-propanediol and 1,4-butanediol are excluded as modifyingdiols. In another embodiment, 2,2-dimethyl-1,3-propanediol is excludedas a modifying diol.

The polyesters and/or the polycarbonates useful in the polyesterscompositions of the invention can comprise from 0 to 10 mole percent,for example, from 0.01 to 5 mole percent, from 0.01 to 1 mole percent,from 0.05 to 5 mole percent, from 0.05 to 1 mole percent, or from 0.1 to0.7 mole percent, based the total mole percentages of either the diol ordiacid residues; respectively, of one or more residues of a branchingmonomer, also referred to herein as a branching agent, having 3 or morecarboxyl substituents, hydroxyl substituents, or a combination thereof.In certain embodiments, the branching monomer or agent may be addedprior to and/or during and/or after the polymerization of the polyester.The polyester(s) useful in the invention can thus be linear or branched.The polycarbonate can also be linear or branched. In certainembodiments, the branching monomer or agent may be added prior to and/orduring and/or after the polymerization of the polycarbonate.

Examples of branching monomers include, but are not limited to,multifunctional acids or multifunctional alcohols such as trimelliticacid, trimellitic anhydride, pyromellitic dianhydride,trimethylolpropane, glycerol, pentaerythritol, citric acid, tartaricacid, 3-hydroxyglutaric acid and the like. In one embodiment, thebranching monomer residues can comprise 0.1 to 0.7 mole percent of oneor more residues chosen from at least one of the following: trimelliticanhydride, pyromellitic dianhydride, glycerol, sorbitol,1,2,6-hexanetriol, pentaerythritol, trimethylolethane, and/or trimesicacid. The branching monomer may be added to the polyester reactionmixture or blended with the polyester in the form of a concentrate asdescribed, for example, in U.S. Pat. Nos. 5,654,347 and 5,696,176, whosedisclosure regarding branching monomers is incorporated herein byreference.

The glass transition temperature (Tg) of the polyesters useful in theinvention was determined using a TA DSC 2920 from Thermal AnalystInstrument at a scan rate of 20° C./min.

Because of the long crystallization half-times (e.g., greater than 5minutes) at 170° C. exhibited by certain polyesters useful in thepresent invention, it can be possible to produce containers injectionblow molded articles, injection stretch blow molded articles, extrusionblow molded articles and extrusion stretch blow molded. The polyestersof the invention can be “amorphous” or semicrystalline. In one aspect,certain polyesters useful in the invention can have a relatively lowcrystallinity. Certain polyesters useful in the invention can thus havea substantially amorphous morphology, meaning that the polyesterscomprise substantially unordered regions of polymer.

In one embodiment, an “amorphous” polyester can have a crystallizationhalf-time of greater than 5 minutes at 170° C. or greater than 10minutes at 170° C. or greater than 50 minutes at 170° C. or greater than100 minutes at 170° C. In one embodiment, of the invention, thecrystallization half-times can be greater than 1,000 minutes at 170° C.In another embodiment of the invention, the crystallization half-timesof the polyesters useful in the invention can be greater than 10,000minutes at 170° C. The crystallization half time of the polyester, asused herein, may be measured using methods well-known to persons ofskill in the art. For example, the crystallization half time of thepolyester, t_(1/2), can be determined by measuring the lighttransmission of a sample via a laser and photo detector as a function oftime on a temperature controlled hot stage. This measurement can be doneby exposing the polymers to a temperature, T_(max), and then cooling itto the desired temperature. The sample can then be held at the desiredtemperature by a hot stage while transmission measurements are made as afunction of time. Initially, the sample can be visually clear with highlight transmission and becomes opaque as the sample crystallizes. Thecrystallization half-time is the time at which the light transmission ishalfway between the initial transmission and the final transmission.T_(max) is defined as the temperature required to melt the crystallinedomains of the sample (if crystalline domains are present). The samplecan be heated to T_(max) to condition the sample prior tocrystallization half time measurement. The absolute T_(max) temperatureis different for each composition. For example PCT can be heated to sometemperature greater than 290° C. to melt the crystalline domains.

As shown in Table 1 and FIG. 1 of the Examples,2,2,4,4-tetramethyl-1,3-cyclobutanediol is more effective than othercomonomers such ethylene glycol and isophthalic acid at increasing thecrystallization half-time, i.e., the time required for a polymer toreach half of its maximum crystallinity. By decreasing thecrystallization rate of PCT, i.e. increasing the crystallizationhalf-time, amorphous articles based on modified PCT may be fabricated bymethods known in the art such as extrusion, injection molding, and thelike. As shown in Table 1, these materials can exhibit higher glasstransition temperatures and lower densities than other modified PCTcopolyesters.

The polyesters can exhibit an improvement in toughness combined withprocessability for some of the embodiments of the invention. Forexample, lowering the inherent viscosity slightly of the polyestersuseful in the invention results in a more processable melt viscositywhile retaining good physical properties of the polyesters such astoughness and heat resistance.

Increasing the content of 1,4-cyclohexanedimethanol in a copolyesterbased on terephthalic acid, ethylene glycol, and1,4-cyclohexanedimethanol can improve toughness which can be determinedby the brittle-to-ductile transition temperature in a notched Izodimpact strength test as measured by ASTM D256. This toughnessimprovement, by lowering of the brittle-to-ductile transitiontemperature with 1,4-cyclohexanedimethanol, is believed to occur due tothe flexibility and conformational behavior of 1,4-cyclohexanedimethanolin the copolyester. Incorporating2,2,4,4-tetramethyl-1,3-cyclobutanediol into PCT is believed to improvetoughness, by lowering the brittle-to-ductile transition temperature, asshown in Table 2 and FIG. 2 of the Examples. This is unexpected giventhe rigidity of 2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In one embodiment, the melt viscosity of the polyester(s) useful in theinvention is less than 30,000 poise as measured a 1 radian/second on arotary melt rheometer at 290° C. In another embodiment, the meltviscosity of the polyester(s) useful in the invention is less than20,000 poise as measured a 1 radian/second on a rotary melt rheometer at290° C.

In one embodiment, the melt viscosity of the polyester(s) useful in theinvention is less than 15,000 poise as measured at 1 radian/second(rad/sec) on a rotary melt rheometer at 290° C. In one embodiment, themelt viscosity of the polyester(s) useful in the invention is less than10,000 poise as measured at 1 radian/second (rad/sec) on a rotary meltrheometer at 290° C. In another embodiment, the melt viscosity of thepolyester(s) useful in the invention is less than 6,000 poise asmeasured at 1 radian/second on a rotary melt rheometer at 290° C.Viscosity at rad/sec is related to processability. Typical polymers haveviscosities of less than 10,000 poise as measured at 1 radian/secondwhen measured at their processing temperature. Polyesters are typicallynot processed above 290 C. Polycarbonate is typically processed at 29°C. The viscosity at 1 rad/sec of a typical 12 melt flow ratepolycarbonate is 7000 poise at 29° C.

In one embodiment, certain polyesters useful in this invention can bevisually clear. The term “visually clear” is defined herein as anappreciable absence of cloudiness, haziness, and/or muddiness, wheninspected visually. In another embodiment, when the polyesters areblended with polycarbonate, including but not limited to, bisphenol Apolycarbonates, the blends can be visually clear.

In other embodiments of the invention, the polyesters useful in theinvention may have a yellowness index (ASTM D-1925) of less than 50 orless than 20.

In one embodiment, the polyesters useful in the invention and/or thepolyester compositions of the invention, with or without toners, canhave color values L*, a* and b* which were determined using a Hunter LabUltrascan Spectra Colorimeter manufactured by Hunter Associates LabInc., Reston, Va. The color determinations are averages of valuesmeasured on either pellets of the polyesters or plaques or other itemsinjection molded or extruded from them. They are determined by theL*a*b* color system of the CIE (International Commission onIllumination) (translated), wherein L* represents the lightnesscoordinate, a* represents the red/green coordinate, and b* representsthe yellow/blue coordinate. In certain embodiments, the b* values forthe polyesters useful in the invention can be from −10 to less than 10and the L* values can be from 50 to 90. In other embodiments, the b*values for the polyesters useful in the invention can be present in oneof the following ranges: from −10 to 9; −10 to 8; −10 to 7; −10 to 6;−10 to 5; −10 to 4; −10 to 3; −10 to 2; from −5 to 9; −5 to 8; −5 to 7;−5 to 6; −5 to 5; −5 to 4; −5 to 3; −5 to 2; 0 to 9; 0 to 8; 0 to 7; 0to 6; 0 to 5; 0 to 4; 0 to 3; 0 to 2; 1 to 10; 1 to 9; 1 to 8; 1 to 7; 1to 6; 1 to 5; 1 to 4; 1 to 3; and 1 to 2. In other embodiments, the L*value for the polyesters useful in the invention can be present in oneof the following ranges: 50 to 60; 50 to 70; 50 to 80; 50 to 90; 60 to70; 60 to 80; 60 to 90; 70 to 80; 79 to 90.

In some embodiments, use of the polyester compositions useful in theinvention minimizes and/or eliminates the drying step prior to meltprocessing and/or thermoforming.

The present polyesters useful in this invention can possess one or moreof the following properties. Notched Izod impact strength, as describedin ASTM D256, is a common method of measuring toughness. The presentpolyesters useful in this invention can possess one or more of thefollowing properties. In one embodiment, the polyesters useful in theinvention exhibit a impact strength of at least 150 J/m (3 ft-lb/in) at23° C. with a 10-mil notch in a 3.2 mm (⅛-inch) thick bar determinedaccording to ASTM D256; in one embodiment, the polyesters useful in theinvention exhibit a notched Izod impact strength of at least (400 J/m)7.5 ft-lb/in at 23° C. with a 10-mil notch in a 3.2 mm (⅛-inch) thickbar determined according to ASTM D256; in one embodiment, the polyestersuseful in the invention exhibit a notched Izod impact strength of atleast 1000 J/m (18 ft-lb/in) at 23° C. with a 10-mil notch in a 3.2 mm(⅛-inch) thick bar determined according to ASTM D256. In one embodiment,the polyesters useful in the invention exhibit a notched Izod impactstrength of at least 150 J/m (3 ft-lb/in) at 23° C. with a 10-mil notchin a 6.4 mm (¼-inch) thick bar determined according to ASTM D256; in oneembodiment, the polyesters useful in the invention exhibit a notchedIzod impact strength of at least (400 J/m) 7.5 ft-lb/in at 23° C. with a10-mil notch in a 6.4 mm (¼-inch) thick bar determined according to ASTMD256; in one embodiment, the polyesters useful in the invention exhibita notched Izod impact strength of at least 1000 J/m (18 ft-lb/in) at 23°C. with a 10-mil notch in a 6.4 mm (⅛-inch) thick bar determinedaccording to ASTM D256.

In another embodiment, certain polyesters useful in the invention canexhibit an increase in notched Izod impact strength when measured at 0°C. of at least 3% or at least 5% or at least 10% or at least 15% ascompared to the notched Izod impact strength when measured at −5° C.with a 10-mil notch in a ⅛-inch thick bar determined according to ASTMD256. In addition, certain other polyesters useful in the invention canalso exhibit a retention of notched Izod impact strength within plus orminus 5% when measured at 0° C. through 30° C. with a 10-mil notch in a⅛-inch thick bar determined according to ASTM D256.

In yet another embodiment, certain polyesters useful in the inventioncan exhibit a retention in notched Izod impact strength with a loss ofno more than 70% when measured at 23° C. with a 10-mil notch in a ¼-inchthick bar determined according to ASTM D256 as compared to notched Izodimpact strength for the same polyester when measured at the sametemperature with a 10-mil notch in a ⅛-inch thick bar determinedaccording to ASTM D256.

In one embodiment, the polyesters useful in the invention can exhibit aductile-to-brittle transition temperature of less than 0° C. based on a10-mil notch in a ⅛-inch thick bar as defined by ASTM D256.

In one embodiment, the polyesters useful in the invention can exhibit atleast one of the following densities: a density of less than 1.2 g/ml at23° C.; a density of less than 1.18 g/ml at 23° C.; a density of 0.70 to1.2 g/ml at 23° C.; a density of 0.70 to 1.3 g/ml at 23° C.; a densityof 0.70 to less than 1.2 g/ml at 23° C.; a density of 0.75 to 1.2 at 23°C.; a density of 0.75 g/ml to less than 1.2 at 23° C.; a density of 0.80g/ml to 1.2 at 23° C.; a density of 0.80 to less than 1.2 g/ml at 23°C.; a density of 0.90 to 1.2 g/ml at 23° C.; a density of 1.0 to 1.2g/ml at 23° C.; a density of 1.0 to 1.3 g/ml at 23° C. a density of 1.1to 1.2 g/ml at 23° C.; a density of 1.13 to 1.3 g/ml at 23° C. a densityof 1.13 to 1.2 g/ml at 23° C.; a density of 0.80 to 1.18 at 23° C.; adensity of 0.80 to less than 1.18 g/ml at 23° C.; a density of 1.0 toless than 1.18 g/ml at 23° C.; a density of 1.1 to less than 1.18 g/mlat 23° C.

In one embodiment, polyesters of this invention exhibit superior notchedtoughness in thick sections. Notched Izod impact strength, as describedin ASTM D256, is a common method of measuring toughness. When tested bythe Izod method, polymers can exhibit either a complete break failuremode, where the test specimen breaks into two distinct parts, or apartial or no break failure mode, where the test specimen remains as onepart. The complete break failure mode is associated with low energyfailure. The partial and no break failure modes are associated with highenergy failure. A typical thickness used to measure Izod toughness is⅛″. At this thickness, very few polymers are believed to exhibit apartial or no break failure mode, polycarbonate being one notableexample. When the thickness of the test specimen is increased to ¼″,however, no commercial amorphous materials exhibit a partial or no breakfailure mode. In one embodiment, compositions of the present exampleexhibit a no break failure mode when tested in Izod using a ¼″ thickspecimen.

In some embodiments, use of the polyester compositions useful in theinvention minimizes and/or eliminates the drying step prior to meltprocessing and/or thermoforming.

The polyester portion of the polyester compositions useful in theinvention can be made by processes known from the literature such as,for example, by processes in homogenous solution, by transesterificationprocesses in the melt, and by two phase interfacial processes. Suitablemethods include, but are not limited to, the steps of reacting one ormore dicarboxylic acids with one or more glycols at a temperature of100° C. to 315° C. at a pressure of 0.1 to 760 mm Hg for a timesufficient to form a polyester. See U.S. Pat. No. 3,772,405 for methodsof producing polyesters, the disclosure regarding such methods is herebyincorporated herein by reference.

In another aspect, the invention relates to containers comprising apolyester produced by a process comprising:

(I) heating a mixture comprising the monomers useful in any of thepolyesters useful in the invention in the presence of a catalyst at atemperature of 150 to 240° C. for a time sufficient to produce aninitial polyester;

(II) heating the initial polyester of step (I) at a temperature of 240to 320° C. for 1 to 4 hours; and

(III) removing any unreacted glycols.

Suitable catalysts for use in this process include, but are not limitedto, organo-zinc or tin compounds. The use of this type of catalyst iswell known in the art. Examples of catalysts useful in the presentinvention include, but are not limited to, zinc acetate, butyltintris-2-ethylhexanoate, dibutyltin diacetate, and dibutyltin oxide. Othercatalysts may include, but are not limited to, those based on titanium,zinc, manganese, lithium, germanium, and cobalt. Catalyst amounts canrange from 10 ppm to 20,000 ppm or 10 to 10,000 ppm, or 10 to 5000 ppmor 10 to 1000 ppm or 10 to 500 ppm, or 10 to 300 ppm or 10 to 250 basedon the catalyst metal and based on the weight of the final polymer. Theprocess can be carried out in either a batch or continuous process.

Typically, step (I) can be carried out until 50% by weight or more ofthe 2,2,4,4-tetramethyl-1,3-cyclobutanediol has been reacted. Step (I)may be carried out under pressure, ranging from atmospheric pressure to100 psig. The term “reaction product” as used in connection with any ofthe catalysts useful in the invention refers to any product of apolycondensation or esterification reaction with the catalyst and any ofthe monomers used in making the polyester as well as the product of apolycondensation or esterification reaction between the catalyst and anyother type of additive.

Typically, Step (II) and Step (III) can be conducted at the same time.These steps can be carried out by methods known in the art such as byplacing the reaction mixture under a pressure ranging, from 0.002 psigto below atmospheric pressure, or by blowing hot nitrogen gas over themixture.

The invention further relates to a polyester product made by the processdescribed above.

The invention further relates to a polymer blend. The blend comprises:

(a) from 5 to 95 wt % of at least one of the polyesters described above;and

(b) from 5 to 95 wt % of at least one of the polymeric components.

Suitable examples of the polymeric components include, but are notlimited to, nylon; polyesters different than those described herein;polyamides such as ZYTEL® from DuPont; polystyrene; polystyrenecopolymers; styrene acrylonitrile copolymers; acrylonitrile butadienestyrene copolymers; poly(methylmethacrylate); acrylic copolymers;poly(ether-imides) such as ULTEM® (a poly(ether-imide) from GeneralElectric); polyphenylene oxides such as poly(2,6-dimethylphenyleneoxide) or poly(phenylene oxide)/polystyrene blends such as NORYL 1000®(a blend of poly(2,6-dimethylphenylene oxide) and polystyrene resinsfrom General Electric); polyphenylene sulfides; polyphenylenesulfide/sulfones; poly(ester-carbonates); polycarbonates such as LEXAN®(a polycarbonate from General Electric); polysulfones; polysulfoneethers; and poly(ether-ketones) of aromatic dihydroxy compounds; ormixtures of any of the foregoing polymers. The blends can be prepared byconventional processing techniques known in the art, such as meltblending or solution blending. In one embodiment, polycarbonate is notpresent in the polyester composition. If polycarbonate is used in ablend in the polyester compositions of the invention, the blends can bevisually clear. However, polyester compositions useful in the inventionalso contemplate the exclusion of polycarbonate as well as the inclusionof polycarbonate.

Polycarbonates useful in the invention may be prepared according toknown procedures, for example, by reacting the dihydroxyaromaticcompound with a carbonate precursor such as phosgene, a haloformate or acarbonate ester, a molecular weight regulator, an acid acceptor and acatalyst. Methods for preparing polycarbonates are known in the art andare described, for example, in U.S. Pat. No. 4,452,933, where thedisclosure regarding the preparation of polycarbonates is herebyincorporated by reference herein.

Examples of suitable carbonate precursors include, but are not limitedto, carbonyl bromide, carbonyl chloride, or mixtures thereof; diphenylcarbonate; a di(halophenyl)carbonate, e.g.,di(trichlorophenyl)carbonate, di(tribromophenyl)carbonate, and the like;di(alkylphenyl)carbonate, e.g., di(tolyl)carbonate;di(naphthyl)carbonate; di(chloronaphthyl)carbonate, or mixtures thereof;and bis-haloformates of dihydric phenols.

Examples of suitable molecular weight regulators include, but are notlimited to, phenol, cyclohexanol, methanol, alkylated phenols, such asoctylphenol, para-tertiary-butyl-phenol, and the like. In oneembodiment, the molecular weight regulator is phenol or an alkylatedphenol.

The acid acceptor may be either an organic or an inorganic acidacceptor. A suitable organic acid acceptor can be a tertiary amine andincludes, but is not limited to, such materials as pyridine,triethylamine, dimethylaniline, tributylamine, and the like. Theinorganic acid acceptor can be either a hydroxide, a carbonate, abicarbonate, or a phosphate of an alkali or alkaline earth metal.

The catalysts that can be used include, but are not limited to, thosethat typically aid the polymerization of the monomer with phosgene.Suitable catalysts include, but are not limited to, tertiary amines suchas triethylamine, tripropylamine, N,N-dimethylaniline, quaternaryammonium compounds such as, for example, tetraethylammonium bromide,cetyl triethyl ammonium bromide, tetra-n-heptylammonium iodide,tetra-n-propyl ammonium bromide, tetramethyl ammonium chloride,tetra-methyl ammonium hydroxide, tetra-n-butyl ammonium iodide,benzyltrimethyl ammonium chloride and quaternary phosphonium compoundssuch as, for example, n-butyltriphenyl phosphonium bromide andmethyltriphenyl phosphonium bromide.

The polycarbonates useful in the polyester compositions of the inventionalso may be copolyestercarbonates such as those described in U.S. Pat.Nos. 3,169,121; 3,207,814; 4,194,038; 4,156,069; 4,430,484, 4,465,820,and 4,981,898, where the disclosure regarding copolyestercarbonates fromeach of the U.S. Patents is incorporated by reference herein.

Copolyestercarbonates useful in this invention can be availablecommercially and/or may be prepared by known methods in the art. Forexample, they can be typically obtained by the reaction of at least onedihydroxyaromatic compound with a mixture of phosgene and at least onedicarboxylic acid chloride, especially isophthaloyl chloride,terephthaloyl chloride, or both.

In addition, the polyester compositions and the polymer blendcompositions useful in the containers of this invention may also containfrom 0.01 to 25% by weight of the overall composition common additivessuch as colorants, dyes, mold release agents, flame retardants,plasticizers, nucleating agents, stabilizers, including but not limitedto, UV stabilizers, thermal stabilizers and/or reaction productsthereof, fillers, and impact modifiers. Examples of typical commerciallyavailable impact modifiers well known in the art and useful in thisinvention include, but are not limited to, ethylene/propyleneterpolymers, functionalized polyolefins such as those containing methylacrylate and/or glycidyl methacrylate, styrene-based block copolymericimpact modifiers, and various acrylic core/shell type impact modifiers.Residues of such additives are also contemplated as part of thepolyester composition

The polyesters of the invention can comprise at least one chainextender. Suitable chain extenders include, but are not limited to,multifunctional (including, but not limited to, bifunctional)isocyanates, multifunctional epoxides, including for example, epoxylatednovolacs, and phenoxy resins. In certain embodiments, chain extendersmay be added at the end of the polymerization process or after thepolymerization process. If added after the polymerization process, chainextenders can be incorporated by compounding or by addition duringconversion processes such as injection molding or extrusion. The amountof chain extender used can vary depending on the specific monomercomposition used and the physical properties desired but is generallyabout 0.1 percent by weight to about 10 percent by weight, such as about0.1 to about 5 percent by weight, based on the total weight of thepolyester.

Thermal stabilizers are compounds that stabilize polyesters duringpolyester manufacture and/or post polymerization, including but notlimited to phosphorous compounds including but not limited to phosphoricacid, phosphorous acid, phosphonic acid, phosphinic acid, phosphonousacid, and various esters and salts thereof. These can be present in thepolyester compositions useful in the invention. The esters can be alkyl,branched alkyl, substituted alkyl, difunctional alkyl, alkyl ethers,aryl, and substituted aryl. In one embodiment, the number of estergroups present in the particular phosphorous compound can vary from zeroup to the maximum allowable based on the number of hydroxyl groupspresent on the thermal stabilizer used. The term “thermal stabilizer” isintended to include the reaction product(s) thereof. The term “reactionproduct” as used in connection with the thermal stabilizers of theinvention refers to any product of a polycondensation or esterificationreaction between the thermal stabilizer and any of the monomers used inmaking the polyester as well as the product of a polycondensation oresterification reaction between the catalyst and any other type ofadditive.

Reinforcing materials may be useful in the compositions of thisinvention. The reinforcing materials may include, but are not limitedto, carbon filaments, silicates, mica, clay, talc, titanium dioxide,Wollastonite, glass flakes, glass beads and fibers, and polymeric fibersand combinations thereof. In one embodiment, the reinforcing materialsinclude glass, such as, fibrous glass filaments, mixtures of glass andtalc, glass and mica, and glass and polymeric fibers.

The invention further relates to containers described herein. Themethods of forming the polyesters into containers are well known in theart.

The invention further relates to bottles described herein. The methodsof forming the polyesters into bottles are well known in the art.Examples of bottles include but are not limited to bottles such as babybottles; water bottles; juice bottles; large commercial water bottleshaving a weight from 200 to 800 grams; beverage bottles which includebut are not limited to two liter bottles, 20 ounce bottles, 16.9 ouncebottles; medical bottles; personal care bottles, carbonated soft drinkbottles; hot fill bottles; water bottles; alcoholic beverage bottlessuch as beer bottles and wine bottles; and bottles comprising at leastone handle. These bottles include but are not limited to injection blowmolded bottles, injection stretch blow molded bottles, extrusion blowmolded bottles, and extrusion stretch blow molded bottles. Methods ofmaking bottles include but are not limited to extrusion blow molding,extrusion stretch blow molding, injection blow molding, and injectionstretch blow molding. In each case, the invention further relates to thepreforms (or parisons) used to make each of said bottles.

These bottles include, but are not limited to, injection blow moldedbottles, injection stretch blow molded bottles, extrusion blow moldedbottles, and extrusion stretch blow molded bottles. Methods of makingbottles include but are not limited to extrusion blow molding, extrusionstretch blow molding, thermoforming, injection blow molding, andinjection stretch blow molding.

Other examples of containers include, but are not limited to, containersfor cosmetics and personal care applications including bottles, jars,vials and tubes; sterilization containers; buffet steam pans; food pansor trays; frozen food trays; microwaveable food trays; hot fillcontainers, amorphous lids or sheets to seal or cover food trays; foodstorage containers; for example, boxes; tumblers, pitchers, cups, bowls,including but not limited to those used in restaurant smallware;beverage containers; retort food containers; centrifuge bowls; vacuumcleaner canisters, and collection and treatment canisters.

For the purposes of this invention, the term “wt” means “weight”.

The following examples further illustrate how the containers of theinvention can be made and evaluated, and are intended to be purelyexemplary of the invention and are not intended to limit the scopethereof. Unless indicated otherwise, parts are parts by weight,temperature is in degrees C. or is at room temperature, and pressure isat or near atmospheric.

EXAMPLES Measurement Methods

The inherent viscosity of the polyesters was determined in 60/40 (wt/wt)phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at 25° C.

Unless stated otherwise, the glass transition temperature (T_(g)) wasdetermined using a TA DSC 2920 instrument from Thermal AnalystInstruments at a scan rate of 20° C./min according to ASTM D3418.

The glycol content and the cis/trans ratio of the compositions weredetermined by proton nuclear magnetic resonance (NMR) spectroscopy. AllNMR spectra were recorded on a JEOL Eclipse Plus 600 MHz nuclearmagnetic resonance spectrometer using either chloroform-trifluoroaceticacid (70-30 volume/volume) for polymers or, for oligomeric samples,60/40 (wt/wt) phenol/tetrachloroethane with deuterated chloroform addedfor lock. Peak assignments for 2,2,4,4-tetramethyl-1,3-cyclobutanediolresonances were made by comparison to model mono- and dibenzoate estersof 2,2,4,4-tetramethyl-1,3-cyclobutanediol. These model compoundsclosely approximate the resonance positions found in the polymers andoligomers.

The crystallization half-time, t½, was determined by measuring the lighttransmission of a sample via a laser and photo detector as a function oftime on a temperature controlled hot stage. This measurement was done byexposing the polymers to a temperature, T_(max), and then cooling it tothe desired temperature. The sample was then held at the desiredtemperature by a hot stage while transmission measurements were made asa function of time. Initially, the sample was visually clear with highlight transmission and became opaque as the sample crystallized. Thecrystallization half-time was recorded as the time at which the lighttransmission was halfway between the initial transmission and the finaltransmission. T_(max) is defined as the temperature required to melt thecrystalline domains of the sample (if crystalline domains are present).The T_(max) reported in the examples below represents the temperature atwhich each sample was heated to condition the sample prior tocrystallization half time measurement. The T_(max) temperature isdependant on composition and is typically different for each polyester.For example, PCT may need to be heated to some temperature greater than290° C. to melt the crystalline domains.

Density was determined using a gradient density column at 23° C.

The melt viscosity reported herein was measured by using a RheometricsDynamic Analyzer (RDA II). The melt viscosity was measured as a functionof shear rate, at frequencies ranging from 1 to 400 rad/sec, at thetemperatures reported. The zero shear melt viscosity (η_(o)) is the meltviscosity at zero shear rate estimated by extrapolating the data byknown models in the art. This step is automatically performed by theRheometrics Dynamic Analyzer (RDA II) software.

The polymers were dried at a temperature ranging from 80 to 100° C. in avacuum oven for 24 hours and injection molded on a Boy 22S moldingmachine to give ⅛×½×5-inch and ¼×½×5-inch flexure bars. These bars werecut to a length of 2.5 inch and notched down the ½ inch width with a10-mil notch in accordance with ASTM D256. The average Izod impactstrength at 23° C. was determined from measurements on 5 specimens.

In addition, 5 specimens were tested at various temperatures using 5° C.increments in order to determine the brittle-to-ductile transitiontemperature. The brittle-to-ductile transition temperature is defined asthe temperature at which 50% of the specimens fail in a brittle manneras denoted by ASTM D256.

Color values reported herein were determined using a Hunter LabUltrascan Spectra Colorimeter manufactured by Hunter Associates LabInc., Reston, Va. The color determinations were averages of valuesmeasured on either pellets of the polyesters or plaques or other itemsinjection molded or extruded from them. They were determined by theL*a*b* color system of the CIE (International Commission onIllumination) (translated), wherein L* represents the lightnesscoordinate, a* represents the red/green coordinate, and b* representsthe yellow/blue coordinate.

In addition, 10-mil films were compression molded using a Carver pressat 240° C.

Unless otherwise specified, the cis/trans ratio of the 1,4cyclohexanedimethanol used in the following examples was approximately30/70, and could range from 35/65 to 25/75. Unless otherwise specified,the cis/trans ratio of the 2,2,4,4-tetramethyl-1,3-cyclobutanediol usedin the following examples was approximately 50/50.

The following abbreviations apply throughout the working examples andfigures:

TPA Terephthalic acid DMT Dimethyl terephthalate TMCD2,2,4,4-tetramethyl-1,3-cyclobutanediol CHDM 1,4-cyclohexanedimethanolIV Inherent viscosity η_(o) Zero shear melt viscosity T_(g) Glasstransition temperature T_(bd) Brittle-to-ductile transition temperatureT_(max) Conditioning temperature for crystallization half timemeasurements

Example 1

This example illustrates that 2,2,4,4-tetramethyl-1,3-cyclobutanediol ismore effective at reducing the crystallization rate of PCT than ethyleneglycol or isophthalic acid. In addition, this example illustrates thebenefits of 2,2,4,4-tetramethyl-1,3-cyclobutanediol on the glasstransition temperature and density.

A variety of copolyesters were prepared as described below. Thesecopolyesters were all made with 200 ppm dibutyl tin oxide as thecatalyst in order to minimize the effect of catalyst type andconcentration on nucleation during crystallization studies. Thecis/trans ratio of the 1,4-cyclohexanedimethanol was 31/69 while thecis/trans ratio of the 2,2,4,4-tetramethyl-1,3-cyclobutanediol isreported in Table 1.

For purposes of this example, the samples had sufficiently similarinherent viscosities thereby effectively eliminating this as a variablein the crystallization rate measurements.

Crystallization half-time measurements from the melt were made attemperatures from 140 to 200° C. at 10° C. increments and are reportedin Table 1. The fastest crystallization half-time for each sample wastaken as the minimum value of crystallization half-time as a function oftemperature, typically occurring around 170 to 180° C. The fastestcrystallization half-times for the samples are plotted in FIG. 1 as afunction of mole % comonomer modification to PCT.

The data shows that 2,2,4,4-tetramethyl-1,3-cyclobutanediol is moreeffective than ethylene glycol and isophthalic acid at decreasing thecrystallization rate (i.e., increasing the crystallization half-time).In addition, 2,2,4,4-tetramethyl-1,3-cyclobutanediol increases T_(g) andlowers density.

TABLE 1 Crystallization Half-times (min) at at at at at at at ComonomerIV Density T_(g) T_(max) 140° C. 150° C. 160° C. 170° C. 180° C. 190° C.200° C. Example (mol %)¹ (dl/g) (g/ml) (° C.) (° C.) (min) (min) (min)(min) (min) (min) (min) 1A 20.2% A² 0.630 1.198 87.5 290 2.7 2.1 1.3 1.20.9 1.1 1.5 1B 19.8% B 0.713 1.219 87.7 290 2.3 2.5 1.7 1.4 1.3 1.4 1.71C 20.0% C 0.731 1.188 100.5 290 >180 >60 35.0 23.3 21.7 23.3 25.2 1D40.2% A² 0.674 1.198 81.2 260 18.7 20.0 21.3 25.0 34.0 59.9 96.1 1E34.5% B 0.644 1.234 82.1 260 8.5 8.2 7.3 7.3 8.3 10.0 11.4 1F 40.1% C0.653 1.172 122.0 260 >10 days >5 days >5 days 19204 >5 days >5 days >5days 1G 14.3% D 0.646³ 1.188 103.0 290 55.0 28.8 11.6 6.8 4.8 5.0 5.5 1H15.0% E 0.728⁴ 1.189 99.0 290 25.4 17.1 8.1 5.9 4.3 2.7 5.1 ¹The balanceof the diol component of the polyesters in Table 1 is1,4-cyclohexanedimethanol; and the balance of the dicarboxylic acidcomponent of the polyesters in Table 1 is dimethyl terephthalate; if thedicarboxylic acid is not described, it is 100 mole % dimethylterephthalate. ²100 mole % 1,4-cyclohexanedimethanol. ³A film waspressed from the ground polyester of Example 1G at 240° C. The resultingfilm had an inherent viscosity value of 0.575 dL/g. ⁴A film was pressedfrom the ground polyester of Example 1H at 240° C. The resulting filmhad an inherent viscosity value of 0.0.652 dL/g. where: A is IsophthalicAcid B is Ethylene Glycol C is 2,2,4,4-Tetramethyl-1,3-cyclobutanediol(approx. 50/50 cis/trans) D is 2,2,4,4-Tetramethyl-1,3-cyclobutanediol(98/2 cis/trans) E is 2,2,4,4-Tetramethyl-1,3-cyclobutanediol (5/95cis/trans)

As shown in Table 1 and FIG. 1, 2,2,4,4-tetramethyl-1,3-cyclobutanediolis more effective than other comonomers, such ethylene glycol andisophthalic acid, at increasing the crystallization half-time, i.e., thetime required for a polymer to reach half of its maximum crystallinity.By decreasing the crystallization rate of PCT (increasing thecrystallization half-time), amorphous articles based on2,2,4,4-tetramethyl-1,3-cyclobutanediol-modified PCT as described hereinmay be fabricated by methods known in the art. As shown in Table 1,these materials can exhibit higher glass transition temperatures andlower densities than other modified PCT copolyesters.

Preparation of the polyesters shown on Table 1 is described below.

Example 1A

This example illustrates the preparation of a copolyester with a targetcomposition of 80 mol % dimethyl terephthalate residues, 20 mol %dimethyl isophthalate residues, and 100 mol % 1,4-cyclohexanedimethanolresidues (28/72 cis/trans).

A mixture of 56.63 g of dimethyl terephthalate, 55.2 g of1,4-cyclohexanedimethanol, 14.16 g of dimethyl isophthalate, and 0.0419g of dibutyl tin oxide was placed in a 500-milliliter flask equippedwith an inlet for nitrogen, a metal stirrer, and a short distillationcolumn. The flask was placed in a Wood's metal bath already heated to210° C. The stirring speed was set to 200 RPM throughout the experiment.The contents of the flask were heated at 210° C. for 5 minutes and thenthe temperature was gradually increased to 290° C. over 30 minutes. Thereaction mixture was held at 290° C. for 60 minutes and then vacuum wasgradually applied over the next 5 minutes until the pressure inside theflask reached 100 mm of Hg. The pressure inside the flask was furtherreduced to 0.3 mm of Hg over the next 5 minutes. A pressure of 0.3 mm ofHg was maintained for a total time of 90 minutes to remove excessunreacted diols. A high melt viscosity, visually clear and colorlesspolymer was obtained with a glass transition temperature of 87.5° C. andan inherent viscosity of 0.63 dl/g. NMR analysis showed that the polymerwas composed of 100 mol % 1,4-cyclohexanedimethanol residues and 20.2mol % dimethyl isophthalate residues.

Example 1B

This example illustrates the preparation of a copolyester with a targetcomposition of 100 mol % dimethyl terephthalate residues, 20 mol %ethylene glycol residues, and 80 mol % 1,4-cyclohexanedimethanolresidues (32/68 cis/trans).

A mixture of 77.68 g of dimethyl terephthalate, 50.77 g of1,4-cyclohexanedimethanol, 27.81 g of ethylene glycol, and 0.0433 g ofdibutyl tin oxide was placed in a 500-milliliter flask equipped with aninlet for nitrogen, a metal stirrer, and a short distillation column.The flask was placed in a Wood's metal bath already heated to 200° C.The stirring speed was set to 200 RPM throughout the experiment. Thecontents of the flask were heated at 200° C. for 60 minutes and then thetemperature was gradually increased to 210° C. over 5 minutes. Thereaction mixture was held at 210° C. for 120 minutes and then heated upto 280° C. in 30 minutes. Once at 280° C., vacuum was gradually appliedover the next 5 minutes until the pressure inside the flask reached 100mm of Hg. The pressure inside the flask was further reduced to 0.3 mm ofHg over the next 10 minutes. A pressure of 0.3 mm of Hg was maintainedfor a total time of 90 minutes to remove excess unreacted diols. A highmelt viscosity, visually clear and colorless polymer was obtained with aglass transition temperature of 87.7° C. and an inherent viscosity of0.71 dl/g. NMR analysis showed that the polymer was composed of 19.8 mol% ethylene glycol residues.

Example 1C

This example illustrates the preparation of a copolyester with a targetcomposition of 100 mol % dimethyl terephthalate residues, 20 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, and 80 mol %1,4-cyclohexanedimethanol residues (31/69 cis/trans).

A mixture of 77.68 g of dimethyl terephthalate, 48.46 g of1,4-cyclohexanedimethanol, 17.86 g of2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 0.046 g of dibutyl tinoxide was placed in a 500-milliliter flask equipped with an inlet fornitrogen, a metal stirrer, and a short distillation column. Thispolyester was prepared in a manner similar to that described in Example1A. A high melt viscosity, visually clear and colorless polymer wasobtained with a glass transition temperature of 100.5° C. and aninherent viscosity of 0.73 dl/g. NMR analysis showed that the polymerwas composed of 80.5 mol % 1,4-cyclohexanedimethanol residues and 19.5mol % 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Example 1D

This example illustrates the preparation of a copolyester with a targetcomposition of 100 mol % dimethyl terephthalate residues, 40 mol %dimethyl isophthalate residues, and 100 mol % 1,4-cyclohexanedimethanolresidues (28/72 cis/trans).

A mixture of 42.83 g of dimethyl terephthalate, 55.26 g of1,4-cyclohexanedimethanol, 28.45 g of dimethyl isophthalate, and 0.0419g of dibutyl tin oxide was placed in a 500-milliliter flask equippedwith an inlet for nitrogen, a metal stirrer, and a short distillationcolumn. The flask was placed in a Wood's metal bath already heated to210° C. The stirring speed was set to 200 RPM throughout the experiment.The contents of the flask were heated at 210° C. for 5 minutes and thenthe temperature was gradually increased to 290° C. over 30 minutes. Thereaction mixture was held at 290° C. for 60 minutes and then vacuum wasgradually applied over the next 5 minutes until the pressure inside theflask reached 100 mm of Hg. The pressure inside the flask was furtherreduced to 0.3 mm of Hg over the next 5 minutes. A pressure of 0.3 mm ofHg was maintained for a total time of 90 minutes to remove excessunreacted diols. A high melt viscosity, visually clear and colorlesspolymer was obtained with a glass transition temperature of 81.2° C. andan inherent viscosity of 0.67 dl/g. NMR analysis showed that the polymerwas composed of 100 mol % 1,4-cyclohexanedimethanol residues and 40.2mol % dimethyl isophthalate residues.

Example 1E

This example illustrates the preparation of a copolyester with a targetcomposition of 100 mol % dimethyl terephthalate residues, 40 mol %ethylene glycol residues, and 60 mol % 1,4-cyclohexanedimethanolresidues (31/69 cis/trans).

A mixture of 81.3 g of dimethyl terephthalate, 42.85 g of1,4-cyclohexanedimethanol, 34.44 g of ethylene glycol, and 0.0419 g ofdibutyl tin oxide was placed in a 500-milliliter flask equipped with aninlet for nitrogen, a metal stirrer, and a short distillation column.The flask was placed in a Wood's metal bath already heated to 200° C.The stirring speed was set to 200 RPM throughout the experiment. Thecontents of the flask were heated at 200° C. for 60 minutes and then thetemperature was gradually increased to 210° C. over 5 minutes. Thereaction mixture was held at 210° C. for 120 minutes and then heated upto 280° C. in 30 minutes. Once at 280° C., vacuum was gradually appliedover the next 5 minutes until the pressure inside the flask reached 100mm of Hg. The pressure inside the flask was further reduced to 0.3 mm ofHg over the next 10 minutes. A pressure of 0.3 mm of Hg was maintainedfor a total time of 90 minutes to remove excess unreacted diols. A highmelt viscosity, visually clear and colorless polymer was obtained with aglass transition temperature of 82.1° C. and an inherent viscosity of0.64 dl/g. NMR analysis showed that the polymer was composed of 34.5 mol% ethylene glycol residues.

Example 1F

This example illustrates the preparation of a copolyester with a targetcomposition of 100 mol % dimethyl terephthalate residues, 40 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues, and 60 mol %1,4-cyclohexanedimethanol residues (31/69 cis/trans).

A mixture of 77.4 g of dimethyl terephthalate, 36.9 g of1,4-cyclohexanedimethanol, 32.5 g of2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 0.046 g of dibutyl tinoxide was placed in a 500-milliliter flask equipped with an inlet fornitrogen, a metal stirrer, and a short distillation column. The flaskwas placed in a Wood's metal bath already heated to 210° C. The stirringspeed was set to 200 RPM throughout the experiment. The contents of theflask were heated at 210° C. for 3 minutes and then the temperature wasgradually increased to 260° C. over 30 minutes. The reaction mixture washeld at 260° C. for 120 minutes and then heated up to 290° C. in 30minutes. Once at 290° C., vacuum was gradually applied over the next 5minutes until the pressure inside the flask reached 100 mm of Hg. Thepressure inside the flask was further reduced to 0.3 mm of Hg over thenext 5 minutes. A pressure of 0.3 mm of Hg was maintained for a totaltime of 90 minutes to remove excess unreacted diols. A high meltviscosity, visually clear and colorless polymer was obtained with aglass transition temperature of 122° C. and an inherent viscosity of0.65 dl/g. NMR analysis showed that the polymer was composed of 59.9 mol% 1,4-cyclohexanedimethanol residues and 40.1 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Example 1G

This example illustrates the preparation of a copolyester with a targetcomposition of 100 mol % dimethyl terephthalate residues, 20 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues (98/2 cis/trans), and80 mol % 1,4-cyclohexanedimethanol residues (31/69 cis/trans).

A mixture of 77.68 g of dimethyl terephthalate, 48.46 g of1,4-cyclohexanedimethanol, 20.77 g of2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 0.046 g of dibutyl tinoxide was placed in a 500-milliliter flask equipped with an inlet fornitrogen, a metal stirrer, and a short distillation column. The flaskwas placed in a Wood's metal bath already heated to 210° C. The stirringspeed was set to 200 RPM throughout the experiment. The contents of theflask were heated at 210° C. for 3 minutes and then the temperature wasgradually increased to 260° C. over 30 minutes. The reaction mixture washeld at 260° C. for 120 minutes and then heated up to 290° C. in 30minutes. Once at 290° C., vacuum was gradually applied over the next 5minutes until the pressure inside the flask reached 100 mm of Hg and thestirring speed was also reduced to 100 RPM. The pressure inside theflask was further reduced to 0.3 mm of Hg over the next 5 minutes andthe stirring speed was reduced to 50 RPM. A pressure of 0.3 mm of Hg wasmaintained for a total time of 60 minutes to remove excess unreacteddiols. A high melt viscosity, visually clear and colorless polymer wasobtained with a glass transition temperature of 103° C. and an inherentviscosity of 0.65 dl/g. NMR analysis showed that the polymer wascomposed of 85.7 mol % 1,4-cyclohexanedimethanol residues and 14.3 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Example 1H

This example illustrates the preparation of a copolyester with a targetcomposition of 100 mol % dimethyl terephthalate residues, 20 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues (5/95 cis/trans), and80 mol % 1,4-cyclohexanedimethanol residues (31/69 cis/trans).

A mixture of 77.68 g of dimethyl terephthalate, 48.46 g of1,4-cyclohexanedimethanol, 20.77 g of2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 0.046 g of dibutyl tinoxide was placed in a 500-milliliter flask equipped with an inlet fornitrogen, a metal stirrer, and a short distillation column. The flaskwas placed in a Wood's metal bath already heated to 210° C. The stirringspeed was set to 200 RPM at the beginning of the experiment. Thecontents of the flask were heated at 210° C. for 3 minutes and then thetemperature was gradually increased to 260° C. over 30 minutes. Thereaction mixture was held at 260° C. for 120 minutes and then heated upto 290° C. in 30 minutes. Once at 290° C., vacuum was gradually appliedover the next 5 minutes with a set point of 100 mm of Hg and thestirring speed was also reduced to 100 RPM. The pressure inside theflask was further reduced to a set point of 0.3 mm of Hg over the next 5minutes and the stirring speed was reduced to 50 RPM. This pressure wasmaintained for a total time of 60 minutes to remove excess unreacteddiols. It was noted that the vacuum system failed to reach the set pointmentioned above, but produced enough vacuum to produce a high meltviscosity, visually clear and colorless polymer with a glass transitiontemperature of 99° C. and an inherent viscosity of 0.73 dl/g. NMRanalysis showed that the polymer was composed of 85 mol %1,4-cyclohexanedimethanol residues and 15 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Example 2

This example illustrates that 2,2,4,4-tetramethyl-1,3-cyclobutanediolimproves the toughness of PCT-based copolyesters (polyesters containingterephthalic acid and 1,4-cyclohexanedimethanol).

Copolyesters based on 2,2,4,4-tetramethyl-1,3-cyclobutanediol wereprepared as described below. The cis/trans ratio of the1,4-cyclohexanedimethanol was approximately 31/69 for all samples.Copolyesters based on ethylene glycol and 1,4-cyclohexanedimethanol werecommercial polyesters. The copolyester of Example 2A (Eastar PCTG 5445)was obtained from Eastman Chemical Co. The copolyester of Example 2B wasobtained from Eastman Chemical Co. under the trade name Spectar. Example2C and Example 2D were prepared on a pilot plant scale (each a 15-lbbatch) following an adaptation of the procedure described in Example 1Aand having the inherent viscosities and glass transition temperaturesdescribed in Table 2 below. Example 2C was prepared with a target tinamount of 300 ppm (Dibutyltin Oxide). The final product contained 295ppm tin. The color values for the polyester of Example 2C were L*=77.11;a*=−1.50; and b*=5.79. Example 2D was prepared with a target tin amountof 300 ppm (Dibutyltin Oxide). The final product contained 307 ppm tin.The color values for the polyester of Example 2D were L*=66.72;a*=−1.22; and b*=16.28.

Materials were injection molded into bars and subsequently notched forIzod testing. The notched Izod impact strengths were obtained as afunction of temperature and are also reported in Table 2.

For a given sample, the Izod impact strength undergoes a majortransition in a short temperature span. For instance, the Izod impactstrength of a copolyester based on 38 mol % ethylene glycol undergoesthis transition between 15 and 20° C. This transition temperature isassociated with a change in failure mode; brittle/low energy failures atlower temperatures and ductile/high energy failures at highertemperatures. The transition temperature is denoted as thebrittle-to-ductile transition temperature, T_(bd), and is a measure oftoughness. T_(bd) is reported in Table 2 and plotted against mol %comonomer in FIG. 2.

The data shows that adding 2,2,4,4-tetramethyl-1,3-cyclobutanediol toPCT lowers T_(bd) and improves the toughness, as compared to ethyleneglycol, which increases T_(bd) of PCT.

TABLE 2 Notched Izod Impact Energy (ft-lb/in) Comonomer IV T_(g) T_(bd)at −20° at −15° at −10° at −5° at 0° at 5° at 10° at 15° at 20° at 25°at 30° Example (mol %)¹ (dl/g) (° C.) (° C.) C. C. C. C. C. C. C. C. C.C. C. 2A 38.0% B 0.68 86 18 NA NA NA 1.5 NA NA 1.5 1.5 32 32 NA 2B 69.0%B 0.69 82 26 NA NA NA NA NA NA 2.1 NA 2.4 13.7 28.7 2C 22.0% C 0.66 106−5 1.5 NA 12 23   23 NA 23 NA NA NA NA 2D 42.8% C 0.60 133 −12 2.5 2.511 NA 14 NA NA NA NA NA NA ¹The balance of the glycol component of thepolyesters in the Table is 1,4-cyclohexanedimethanol. All polymers wereprepared from 100 mole % dimethyl terephthalate. NA = Not available.where: B is Ethylene glycol C is 2,2,4,4-Tetramethyl-1,3-cyclobutanediol(50/50 cis/trans)

Example 3

This example illustrates that 2,2,4,4-tetramethyl-1,3-cyclobutanediolcan improve the toughness of PCT-based copolyesters (polyesterscontaining terephthalic acid and 1,4-cyclohexanedimethanol). Polyestersprepared in this example comprise from 15 to 25 mol % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Copolyesters based on dimethyl terephthalate,2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 1,4-cyclohexanedimethanolwere prepared as described below, having the composition and propertiesshown on Table 3. The balance up to 100 mol % of the diol component ofthe polyesters in Table 3 was 1,4-cyclohexanedimethanol (31/69cis/trans).

Materials were injection molded into both 3.2 mm and 6.4 mm thick barsand subsequently notched for Izod impact testing. The notched Izodimpact strengths were obtained at 23° C. and are reported in Table 3.Density, Tg, and crystallization halftime were measured on the moldedbars. Melt viscosity was measured on pellets at 290° C.

TABLE 3 Compilation of various properties for certain polyesters usefulin the invention Notched Izod Notched Izod Crystallization MeltViscosity Pellet Molded of 3.2 mm of 6.4 mm Specific Halftime from at 1rad/sec TMCD % cis IV Bar IV thick bars at thick bars at Gravity Tg meltat 170° C. at 290° C. Example mole % TMCD (dl/g) (dl/g) 23° C. (J/m) 23°C. (J/m) (g/mL) (° C.) (min) (Poise) A 15 48.8 0.736 0.707 1069 8781.184 104 15 5649 B 18 NA 0.728 0.715 980 1039 1.183 108 22 6621 C 20 NA0.706 0.696 1006 1130 1.182 106 52 6321 D 22 NA 0.732 0.703 959 9881.178 108 63 7161 E 21 NA 0.715 0.692 932 482 1.179 110 56 6162 F 24 NA0.708 0.677 976 812 1.180 109 58 6282 G 23 NA 0.650 0.610 647 270 1.182107 46 3172 H 23 47.9 0.590 0.549 769 274 1.181 106 47 1736 I 23 48.10.531 0.516 696 352 1.182 105 19 1292 J 23 47.8 0.364 NA NA NA NA 98 NA167 NA = Not available.

Example 3A

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 14.34 lb (45.21gram-mol) 1,4-cyclohexanedimethanol, and 4.58 lb (14.44 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and at a pressure of 20 psig. The pressure was thendecreased to 0 psig at a rate of 3 psig/minute. The temperature of thereaction mixture was then increased to 270° C. and the pressure wasdecreased to 90 mm of Hg. After a 1 hour hold time at 270° C. and 90 mmof Hg, the agitator speed was decreased to 15 RPM, the reaction mixturetemperature was increased to 290° C., and the pressure was decreased to<1 mm of Hg. The reaction mixture was held at 290° C. and at a pressureof <1 mm of Hg until the power draw to the agitator no longer increased(70 minutes). The pressure of the pressure vessel was then increased to1 atmosphere using nitrogen gas. The molten polymer was then extrudedfrom the pressure vessel. The cooled, extruded polymer was ground topass a 6-mm screen. The polymer had an inherent viscosity of 0.736 dL/gand a Tg of 104° C. NMR analysis showed that the polymer was composed of85.4 mol % 1,4-cyclohexane-dimethanol residues and 14.6 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polymer had colorvalues of: L*=78.20, a*=−1.62, and b*=6.23.

Example 3B to Example 3D

The polyesters described in Example 3B to Example 3D were preparedfollowing a procedure similar to the one described for Example 3A. Thecomposition and properties of these polyesters are shown in Table 3.

Example 3E

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 12.61 lb (39.77gram-mol) 1,4-cyclohexanedimethanol, and 6.30 lb (19.88 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. The temperature of the reactionmixture was then increased to 270° C. and the pressure was decreased to90 mm of Hg. After a 1 hour hold time at 270° C. and 90 mm of Hg, theagitator speed was decreased to 15 RPM, the reaction mixture temperaturewas increased to 290° C., and the pressure was decreased to <1 mm of Hg.The reaction mixture was held at 290° C. and at a pressure of <1 mm ofHg for 60 minutes. The pressure of the pressure vessel was thenincreased to 1 atmosphere using nitrogen gas. The molten polymer wasthen extruded from the pressure vessel. The cooled, extruded polymer wasground to pass a 6-mm screen. The polymer had an inherent viscosity of0.715 dL/g and a Tg of 110° C. X-ray analysis showed that the polyesterhad 223 ppm tin. NMR analysis showed that the polymer was composed of78.6 mol % 1,4-cyclohexane-dimethanol residues and 21.4 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polymer had colorvalues of: L*=76.45, a*=−1.65, and b*=6.47.

Example 3F

The polyester described in Example 3F was prepared following a proceduresimilar to the one described for Example 3A. The composition andproperties of this polyester are shown in Table 3.

Example 3G

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 12.61 lb (39.77gram-mol) 1,4-cyclohexanedimethanol, and 6.30 lb (19.88 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. The temperature of the reactionmixture was then increased to 270° C. and the pressure was decreased to90 mm of Hg. After a 1 hour hold time at 270° C. and 90 mm of Hg, theagitator speed was decreased to 15 RPM, the reaction mixture temperaturewas increased to 290° C., and the pressure was decreased to <1 mm of Hg.The reaction mixture was held at 290° C. and at a pressure of <1 mm ofHg for 12 minutes. The pressure of the pressure vessel was thenincreased to 1 atmosphere using nitrogen gas. The molten polymer wasthen extruded from the pressure vessel. The cooled, extruded polymer wasground to pass a 6-mm screen. The polymer had an inherent viscosity of0.590 dL/g and a Tg of 106° C. NMR analysis showed that the polymer wascomposed of 77.1 mol % 1,4-cyclohexane-dimethanol residues and 22.9 mol% 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polymer hadcolor values of: L*=83.27, a*=−1.34, and b*=5.08.

Example 3H

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 12.61 lb (39.77gram-mol) 1,4-cyclohexanedimethanol, and 6.30 lb (19.88 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. The temperature of the reactionmixture was then increased to 270° C. and the pressure was decreased to90 mm of Hg. After a 1 hour hold time at 270° C. and 90 mm of Hg, theagitator speed was decreased to 15 RPM, the reaction mixture temperaturewas increased to 290° C., and the pressure was decreased to 4 mm of Hg.The reaction mixture was held at 290° C. and at a pressure of 4 mm of Hgfor 30 minutes. The pressure of the pressure vessel was then increasedto 1 atmosphere using nitrogen gas. The molten polymer was then extrudedfrom the pressure vessel. The cooled, extruded polymer was ground topass a 6-mm screen. The polymer had an inherent viscosity of 0.531 dL/gand a Tg of 105° C. NMR analysis showed that the polymer was composed of76.9 mol % 1,4-cyclohexane-dimethanol residues and 23.1 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polymer had colorvalues of: L*=80.42, a*=−1.28, and b*=5.13.

Example 3I

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 12.61 lb (39.77gram-mol) 1,4-cyclohexanedimethanol, and 6.30 lb (19.88 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. The temperature of the reactionmixture was then increased to 270° C. and the pressure was decreased to90 mm of Hg. After a 1 hour hold time at 270° C. and 90 mm of Hg, theagitator speed was decreased to 15 RPM, the reaction mixture temperaturewas increased to 290° C., and the pressure was decreased to 4 mm of Hg.When the reaction mixture temperature was 290° C. and the pressure was 4mm of Hg, the pressure of the pressure vessel was immediately increasedto 1 atmosphere using nitrogen gas. The molten polymer was then extrudedfrom the pressure vessel. The cooled, extruded polymer was ground topass a 6-mm screen. The polymer had an inherent viscosity of 0.364 dL/gand a Tg of 98° C. NMR analysis showed that the polymer was composed of77.5 mol % 1,4-cyclohexane-dimethanol residues and 22.5 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polymer had colorvalues of: L*=77.20, a*=−1.47, and b*=4.62.

Example 4

This example illustrates that 2,2,4,4-tetramethyl-1,3-cyclobutanediolcan improve the toughness of PCT-based copolyesters (polyesterscontaining terephthalic acid and 1,4-cyclohexanedimethanol). Polyestersprepared in this example fall comprise more than 25 to less than 40 mol% of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Copolyesters based on dimethyl terephthalate,2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 1,4-cyclohexanedimethanol(31/69 cis/trans) were prepared as described below, having thecomposition and properties shown on Table 4. The balance up to 100 mol %of the diol component of the polyesters in Table 4 was1,4-cyclohexanedimethanol (31/69 cis/trans).

Materials were injection molded into both 3.2 mm and 6.4 mm thick barsand subsequently notched for Izod impact testing. The notched Izodimpact strengths were obtained at 23° C. and are reported in Table 4.Density, Tg, and crystallization halftime were measured on the moldedbars. Melt viscosity was measured on pellets at 290° C.

TABLE 4 Compilation of various properties for certain polyesters usefulin the invention Notched Izod Notched Izod Crystallization MeltViscosity Pellet Molded of 3.2 mm of 6.4 mm Specific Halftime from at 1rad/sec TMCD % cis IV Bar IV thick bars at thick bars at Gravity Tg meltat 170° C. at 290° C. Example mole % TMCD (dl/g) (dl/g) 23° C. (J/m) 23°C. (J/m) (g/mL) (° C.) (min) (Poise) A 27 47.8 0.714 0.678 877 878 1.178113 280 8312 B 31 NA 0.667 0.641 807 789 1.174 116 600 6592 NA = Notavailable.

Example 4A

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 11.82 lb (37.28gram-mol) 1,4-cyclohexanedimethanol, and 6.90 lb (21.77 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. The temperature of the reactionmixture was then increased to 270° C. and the pressure was decreased to90 mm of Hg. After a 1 hour hold time at 270° C. and 90 mm of Hg, theagitator speed was decreased to 15 RPM, the reaction mixture temperaturewas increased to 290° C., and the pressure was decreased to <1 mm of Hg.The reaction mixture was held at 290° C. and at a pressure of <1 mm ofHg until the power draw to the agitator no longer increased (50minutes). The pressure of the pressure vessel was then increased to 1atmosphere using nitrogen gas. The molten polymer was then extruded fromthe pressure vessel. The cooled, extruded polymer was ground to pass a6-mm screen. The polymer had an inherent viscosity of 0.714 dL/g and aTg of 113° C. NMR analysis showed that the polymer was composed of 73.3mol % 1,4-cyclohexane-dimethanol residues and 26.7 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Example 4B

The polyester of Example 4B was prepared following a procedure similarto the one described for Example 4A. The composition and properties ofthis polyester are shown in Table 4.

Example 5

This example illustrates that 2,2,4,4-tetramethyl-1,3-cyclobutanediolcan improve the toughness of PCT-based copolyesters (polyesterscontaining terephthalic acid and 1,4-cyclohexanedimethanol). Polyestersprepared in this example comprise2,2,4,4-tetramethyl-1,3-cyclobutanediol residues in an amount of 40 mol% or greater.

Copolyesters based on dimethyl terephthalate,2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 1,4-cyclohexanedimethanolwere prepared as described below, having the composition and propertiesshown on Table 5. The balance up to 100 mol % of the diol component ofthe polyesters in Table 5 was 1,4-cyclohexanedimethanol (31/69cis/trans).

Materials were injection molded into both 3.2 mm and 6.4 mm thick barsand subsequently notched for Izod impact testing. The notched Izodimpact strengths were obtained at 23° C. and are reported in Table 5.Density, Tg, and crystallization halftime were measured on the moldedbars. Melt viscosity was measured on pellets at 290° C.

TABLE 5 Compilation of various properties for certain polyesters usefulin the invention Notched Izod Notched Izod Crystallization MeltViscosity Pellet Molded of 3.2 mm of 6.4 mm Specific Halftime from at 1rad/sec TMCD % cis IV Bar IV thick bars at thick bars at Gravity Tg meltat 170° C. at 290° C. Example mole % TMCD (dl/g) (dl/g) 23° C. (J/m) 23°C. (J/m) (g/mL) (° C.) (min) (Poise) A 44 46.2 0.657 0.626 727 734 1.172119 NA 9751 B 45 NA 0.626 0.580 748 237 1.167 123 NA 8051 C 45 NA 0.5820.550 671 262 1.167 125 19782 5835 D 45 NA 0.541 0.493 424 175 1.167 123NA 3275 E 59 46.6 0.604 0.576 456 311 1.156 139 NA 16537 F 45 47.2 0.4750.450 128 30 1.169 121 NA 1614 NA = Not available.

Example 5A

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 8.84 lb (27.88gram-mol) 1,4-cyclohexanedimethanol, and 10.08 lb (31.77 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. Then the agitator speed wasdecreased to 15 RPM, the temperature of the reaction mixture was thenincreased to 290° C. and the pressure was decreased to 2 mm of Hg. Thereaction mixture was held at 290° C. and at a pressure of 2 mm of Hguntil the power draw to the agitator no longer increased (80 minutes).The pressure of the pressure vessel was then increased to 1 atmosphereusing nitrogen gas. The molten polymer was then extruded from thepressure vessel. The cooled, extruded polymer was ground to pass a 6-mmscreen. The polymer had an inherent viscosity of 0.657 dL/g and a Tg of119° C. NMR analysis showed that the polymer was composed of 56.3 mol %1,4-cyclohexane-dimethanol residues and 43.7 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polymer had colorvalues of: L*=75.04, a*=−1.82, and b*=6.72.

Example 5B to Example 5D

The polyesters described in Example 5B to Example 5D were preparedfollowing a procedure similar to the one described for Example 5A. Thecomposition and properties of these polyesters are shown in Table 5.

Example 5E

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 6.43 lb (20.28gram-mol 1,4-cyclohexanedimethanol, and 12.49 lb (39.37 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. Then the agitator speed wasdecreased to 15 RPM, the temperature of the reaction mixture was thenincreased to 290° C. and the pressure was decreased to 2 mm of Hg. Thereaction mixture was held at 290° C. and at a pressure of <1 mm of Hguntil the power draw to the agitator no longer increased (50 minutes).The pressure of the pressure vessel was then increased to 1 atmosphereusing nitrogen gas. The molten polymer was then extruded from thepressure vessel. The cooled, extruded polymer was ground to pass a 6-mmscreen. The polymer had an inherent viscosity of 0.604 dL/g and a Tg of139° C. NMR analysis showed that the polymer was composed of 40.8 mol %1,4-cyclohexanedimethanol residues and 59.2 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polymer had colorvalues of: L*=80.48, a*=−1.30, and b*=6.82.

Example 5F

21.24 lb (49.71 gram-mol) dimethyl terephthalate, 8.84 lb (27.88gram-mol) 1,4-cyclohexanedimethanol, and 10.08 lb (31.77 gram-mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol were reacted together in thepresence of 200 ppm of the catalyst butyltin tris(2-ethylhexanoate). Thereaction was carried out under a nitrogen gas purge in an 18-gallonstainless steel pressure vessel fitted with a condensing column, avacuum system, and a HELICONE-type agitator. With the agitator runningat 25 RPM, the reaction mixture temperature was increased to 250° C. andthe pressure was increased to 20 psig. The reaction mixture was held for2 hours at 250° C. and 20 psig pressure. The pressure was then decreasedto 0 psig at a rate of 3 psig/minute. The temperature of the reactionmixture was then increased to 270° C. and the pressure was decreased to90 mm of Hg. After a 1 hour hold time at 270° C. and 90 mm of Hg, theagitator speed was decreased to 15 RPM and the pressure was decreased to4 mm of Hg. When the reaction mixture temperature was 270° C. and thepressure was 4 mm of Hg, the pressure of the pressure vessel wasimmediately increased to 1 atmosphere using nitrogen gas. The moltenpolymer was then extruded from the pressure vessel. The cooled, extrudedpolymer was ground to pass a 6-mm screen. The polymer had an inherentviscosity of 0.475 dL/g and a Tg of 121° C. NMR analysis showed that thepolymer was composed of 55.5 mol % 1,4-cyclohexane-dimethanol residuesand 44.5 mol % 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. Thepolymer had color values of: L*=85.63, a*=−0.88, and b*=4.34.

Example 6 Comparative Example

This example shows data for comparative materials are shown in Table 6.The PC was Makrolon 2608 from Bayer, with a nominal composition of 100mole % bisphenol A residues and 100 mole % diphenyl carbonate residues.Makrolon 2608 has a nominal melt flow rate of 20 grams/10 minutesmeasured at 30° C. using a 1.2 kg weight. The PET was Eastar 9921 fromEastman Chemical Company, with a nominal composition of 100 mole %terephthalic acid, 3.5 mole % cyclohexanedimethanol (CHDM) and 96.5 mole% ethylene glycol. The PETG was Eastar 6763 from Eastman ChemicalCompany, with a nominal composition of 100 mole % terephthalic acid, 31mole % cyclohexanedimethanol (CHDM) and 69 mole % ethylene glycol. ThePCTG was Eastar DN001 from Eastman Chemical Company, with a nominalcomposition of 100 mole % terephthalic acid, 62 mole %cyclohexanedimethanol (CHDM) and 38 mole % ethylene glycol. The PCTA wasEastar AN001 from Eastman Chemical Company, with a nominal compositionof 65 mole % terephthalic acid, 35 mole % isophthalic acid and 100 mole% cyclohexanedimethanol (CHDM). The Polysulfone was Udel 1700 fromSolvay, with a nominal composition of 100 mole % bisphenol A residuesand 100 mole % 4,4-dichlorosulfonyl sulfone residues. Udel 1700 has anominal melt flow rate of 6.5 grams/10 minutes measured at 343 C using a2.16 kg weight. The SAN was Lustran 31 from Lanxess, with a nominalcomposition of 76 weight % styrene and 24 weight % acrylonitrile.Lustran 31 has a nominal melt flow rate of 7.5 grams/10 minutes measuredat 23° C. using a 3.8 kg weight. The examples of the invention showimproved toughness in 6.4 mm thickness bars compared to all of the otherresins.

TABLE 6 Compilation of various properties for certain commercialpolymers Notched Izod Notched Izod Pellet Molded of 3.2 mm of 6.4 mmSpecific Crystallization Polymer IV Bar IV thick bars at thick bars atGravity Tg Halftime from Example name (dl/g) (dl/g) 23° C. (J/m) 23° C.(J/m) (g/mL) (° C.) melt (min) A PC  12 MFR NA 929  108  1.20 146 NA BPCTG 0.73 0.696 NB 70 1.23 87 30 at 170° C. C PCTA 0.72 0.702 98 59 1.2087 15 at 150° C. D PETG 0.75 0.692 83 59 1.27 80 2500 at 130° C.  E PET0.76 0.726 45 48 1.33 78 1.5 at 170° C.  F SAN 7.5 MFR NA 21 NA 1.07~110 NA G PSU 6.5 MFR NA 69 NA 1.24 ~190 NA NA = Not available

Example 7

This example illustrates the effect of the amount of2,2,4,4-tetramethyl-1,3-cyclobutanediol used for the preparation of thepolyesters of the invention on the glass transition temperature of thepolyesters. Polyesters prepared in this example comprise from 15 to 25mol % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

Example 7A to Example 7G

Dimethyl terephthalate, 1,4-cyclohexanedimethanol, and2,2,4,4-tetramethyl-1,3-cyclobutanediol were weighed into a 500-mlsingle neck round bottom flask. NMR analysis on the2,2,4,4-tetramethyl-1,3-cyclobutanediol starting material showed acis/trans ratio of 53/47. The polyesters of this example were preparedwith a 1.2/1 glycol/acid ratio with the entire excess coming from the2,2,4,4-tetramethyl-1,3-cyclobutanediol. Enough dibutyltin oxidecatalyst was added to give 300 ppm tin in the final polymer. The flaskwas under a 0.2 SCFC nitrogen purge with vacuum reduction capability.The flask was immersed in a Belmont metal bath at 200° C. and stirred at200 RPM after the reactants had melted. After about 2.5 hours, thetemperature was raised to 210° C. and these conditions were held for anadditional 2 hours. The temperature was raised to 285° C. (inapproximately 25 minutes) and the pressure was reduced to 0.3 mm of Hgover a period of 5 minutes. The stirring was reduced as the viscosityincreased, with 15 RPM being the minimum stirring used. The totalpolymerization time was varied to attain the target inherentviscosities. After the polymerization was complete, the Belmont metalbath was lowered and the polymer was allowed to cool to below its glasstransition temperature. After about 30 minutes, the flask was reimmersedin the Belmont metal bath (the temperature had been increased to 295° C.during this 30 minute wait) and the polymer mass was heated until itpulled away from the glass flask. The polymer mass was stirred at midlevel in the flask until the polymer had cooled. The polymer was removedfrom the flask and ground to pass a 3 mm screen. Variations to thisprocedure were made to produce the copolyesters described below with atargeted composition of 20 mol %.

Inherent viscosities were measured as described in the “MeasurementMethods” section above. The compositions of the polyesters weredetermined by ¹H NMR as explained before in the Measurement Methodssection. The glass transition temperatures were determined by DSC, usingthe second heat after quench at a rate of 20° C./min.

Example 7H to Example 7Q

These polyesters were prepared by carrying out the ester exchange andpolycondensation reactions in separate stages. The ester exchangeexperiments were conducted in a continuous temperature rise (CTR)reactor. The CTR was a 3000 ml glass reactor equipped with a singleshaft impeller blade agitator, covered with an electric heating mantleand fitted with a heated packed reflux condenser column. The reactor wascharged with 777 g (4 moles) of dimethyl terephthalate, 230 g (1.6moles) of 2,2,4,4-tetramethyl-1,3-cyclobutanediol, 460.8 g (3.2 moles)of cyclohexane dimethanol and 1.12 g of butyltin tris-2-ethylhexanoate(such that there will be 200 ppm tin metal in the final polymer). Theheating mantle was set manually to 100% output. The set points and datacollection were facilitated by a Camile process control system. Once thereactants were melted, stirring was initiated and slowly increased to250 rpm. The temperature of the reactor gradually increased with runtime. The weight of methanol collected was recorded via balance. Thereaction was stopped when methanol evolution stopped or at apre-selected lower temperature of 260° C. The oligomer was dischargedwith a nitrogen purge and cooled to room temperature. The oligomer wasfrozen with liquid nitrogen and broken into pieces small enough to beweighed into a 500 ml round bottom flask.

In the polycondensation reactions, a 500 ml round bottom flask wascharged with approximately 150 g of the oligomer prepared above. Theflask was equipped with a stainless steel stirrer and polymer head. Theglassware was set up on a half mole polymer rig and the Camile sequencewas initiated. The stirrer was positioned one full turn from the flaskbottom once the oligomer melted. The temperature/pressure/stir ratesequence controlled by the Camile software for each example is reportedin the following tables.

Camile Sequence for Example 7H and Example 7I

Time Temp Vacuum Stir Stage (min) (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 290 90 50 6 5 290 6 25 7110 290 6 25

Camile Sequence for Example 7N to Example 7Q

Time Temp Vacuum Stir Stage (min) (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 290 90 50 6 5 290 3 25 7110 290 3 25

Camile Sequence for Example 7K and Example 7L

Time Temp Vacuum Stir Stage (min) (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 290 90 50 6 5 290 2 25 7110 290 2 25

Camile Sequence for Example 7J and Example 7M

Time Temp Vacuum Stir Stage (min) (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 290 90 50 6 5 290 1 25 7110 290 1 25

The resulting polymers were recovered from the flask, chopped using ahydraulic chopper, and ground to a 6 mm screen size. Samples of eachground polymer were submitted for inherent viscosity in 60/40 (wt/wt)phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at 25° C.,catalyst level (Sn) by x-ray fluorescence, and color (L*, a*, b*) bytransmission spectroscopy. Polymer composition was obtained by ¹H NMR.Samples were submitted for thermal stability and melt viscosity testingusing a Rheometrics Mechanical Spectrometer (RMS-800).

The table below shows the experimental data for the polyesters of thisexample. The data shows that an increase in the level of2,2,4,4-tetramethyl-1,3-cyclobutanediol raises the glass transitiontemperature in an almost linear fashion, for a constant inherentviscosity. FIG. 3 also shows the dependence of Tg on composition andinherent viscosity.

TABLE 7 Glass transition temperature as a function of inherent viscosityand composition η_(o) at η_(o) at η_(o) at Exam- mol % % cis IV T_(g)260° C. 275° C. 290° C. ple TMCD TMCD (dL/g) (° C.) (Poise) (Poise)(Poise) A 20 51.4 0.72 109 11356 19503 5527 B 19.1 51.4 0.60 106 68913937 2051 C 19 53.2 0.64 107 8072 4745 2686 D 18.8 54.4 0.70 108 149378774 4610 E 17.8 52.4 0.50 103 3563 1225 883 F 17.5 51.9 0.75 107 2116010877 5256 G 17.5 52 0.42 98 NA NA NA H 22.8 53.5 0.69 109 NA NA NA I22.7 52.2 0.68 108 NA NA NA J 23.4 52.4 0.73 111 NA NA NA K 23.3 52.90.71 111 NA NA NA L 23.3 52.4 0.74 112 NA NA NA M 23.2 52.5 0.74 112 NANA NA N 23.1 52.5 0.71 111 NA NA NA O 22.8 52.4 0.73 112 NA NA NA P 22.753 0.69 112 NA NA NA Q 22.7 52 0.70 111 NA NA NA NA = Not available

Example 8

This example illustrates the effect of the amount of2,2,4,4-tetramethyl-1,3-cyclobutanediol used for the preparation of thepolyesters of the invention on the glass transition temperature of thepolyesters. Polyesters prepared in this example fall comprise more than25 to less than 40 mol % of 2,2,4,4-tetramethyl-1,3-cyclobutanediolresidues.

Dimethyl terephthalate, 1,4-cyclohexanedimethanol, and2,2,4,4-tetramethyl-1,3-cyclobutanediol were weighed into a 500-mlsingle neck round bottom flask. NMR analysis on the2,2,4,4-tetramethyl-1,3-cyclobutanediol starting material showed acis/trans ratio of 53/47. The polyesters of this example were preparedwith a 1.2/1 glycol/acid ratio with the entire excess coming from the2,2,4,4-tetramethyl-1,3-cyclobutanediol. Enough dibutyltin oxidecatalyst was added to give 300 ppm tin in the final polymer. The flaskwas under a 0.2 SCFC nitrogen purge with vacuum reduction capability.The flask was immersed in a Belmont metal bath at 200° C. and stirred at200 RPM after the reactants had melted. After about 2.5 hours, thetemperature was raised to 210° C. and these conditions were held for anadditional 2 hours. The temperature was raised to 285° C. (inapproximately 25 minutes) and the pressure was reduced to 0.3 mm of Hgover a period of 5 minutes. The stirring was reduced as the viscosityincreased, with 15 RPM being the minimum stirring used. The totalpolymerization time was varied to attain the target inherentviscosities. After the polymerization was complete, the Belmont metalbath was lowered and the polymer was allowed to cool to below its glasstransition temperature. After about 30 minutes, the flask was reimmersedin the Belmont metal bath (the temperature had been increased to 295° C.during this 30 minute wait) and the polymer mass was heated until itpulled away from the glass flask. The polymer mass was stirred at midlevel in the flask until the polymer had cooled. The polymer was removedfrom the flask and ground to pass a 3 mm screen. Variations to thisprocedure were made to produce the copolyesters described below with atargeted composition of 32 mol %.

Inherent viscosities were measured as described in the “MeasurementMethods” section above. The compositions of the polyesters weredetermined by ¹H NMR as explained before in the Measurement Methodssection. The glass transition temperatures were determined by DSC, usingthe second heat after quench at a rate of 20° C./min.

The table below shows the experimental data for the polyesters of thisexample. FIG. 3 also shows the dependence of Tg on composition andinherent viscosity. The data shows that an increase in the level of2,2,4,4-tetramethyl-1,3-cyclobutanediol raises the glass transitiontemperature in an almost linear fashion, for a constant inherentviscosity.

TABLE 8 Glass transition temperature as a function of inherent viscosityand composition η_(o) at η_(o) at η_(o) at Exam- mol % % cis IV T_(g)260° C. 275° C. 290° C. ple TMCD TMCD (dL/g) (° C.) (Poise) (Poise)(Poise) A 32.2 51.9 0.71 118 29685 16074 8522 B 31.6 51.5 0.55 112 51952899 2088 C 31.5 50.8 0.62 112 8192 4133 2258 D 30.7 50.7 0.54 111 43452434 1154 E 30.3 51.2 0.61 111 7929 4383 2261 F 30.0 51.4 0.74 117 3147617864 8630 G 29.0 51.5 0.67 112 16322 8787 4355 H 31.1 51.4 0.35 102 NANA NA NA = Not available

Example 9

This example illustrates the effect of the amount of2,2,4,4-tetramethyl-1,3-cyclobutanediol used for the preparation of thepolyesters of the invention on the glass transition temperature of thepolyesters. Polyesters prepared in this example comprise2,2,4,4-tetramethyl-1,3-cyclobutanediol residues in an amount of 40 mol% or greater.

Examples A to AC

These polyesters were prepared by carrying out the ester exchange andpolycondensation reactions in separate stages. The ester exchangeexperiments were conducted in a continuous temperature rise (CTR)reactor. The CTR was a 3000 ml glass reactor equipped with a singleshaft impeller blade agitator, covered with an electric heating mantleand fitted with a heated packed reflux condenser column. The reactor wascharged with 777 g of dimethyl terephthalate, 375 g of2,2,4,4-tetramethyl-1,3-cyclobutanediol, 317 g of cyclohexane dimethanoland 1.12 g of butyltin tris-2-ethylhexanoate (such that there will be200 ppm tin metal in the final polymer). The heating mantle was setmanually to 100% output. The set points and data collection werefacilitated by a Camile process control system. Once the reactants weremelted, stirring was initiated and slowly increased to 250 rpm. Thetemperature of the reactor gradually increased with run time. The weightof methanol collected was recorded via balance. The reaction was stoppedwhen methanol evolution stopped or at a pre-selected lower temperatureof 260° C. The oligomer was discharged with a nitrogen purge and cooledto room temperature. The oligomer was frozen with liquid nitrogen andbroken into pieces small enough to be weighed into a 500 ml round bottomflask.

In the polycondensation reactions, a 500 ml round bottom flask wascharged with 150 g of the oligomer prepared above. The flask wasequipped with a stainless steel stirrer and polymer head. The glasswarewas set up on a half mole polymer rig and the Camile sequence wasinitiated. The stirrer was positioned one full turn from the flaskbottom once the oligomer melted. The temperature/pressure/stir ratesequence controlled by the Camile software for these examples isreported in the following table, unless otherwise specified below.

Camile Sequence for Polycondensation Reactions

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 290 90 50 6 5 290 6 25 7110 290 6 25

Camile Sequence for Examples A, C, R, Y, AB, AC

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 290 90 50 6 5 290 6 25 7110 290 6 25

For Examples B, D, F, the same sequence in the preceding table was used,except the time was 80 min in Stage 7. For Examples G and J, the samesequence in the preceding table was used, except the time was 50 min inStage 7. For Example L, the same sequence in the preceding table wasused, except the time was 140 min in Stage 7.

Camile Sequence for Example E

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 300 90 50 6 5 300 7 25 7110 300 7 25

For Example I, the same sequence in the preceding table was used, exceptthe vacuum was 8 torr in Stages 6 and 7. For Example O, the samesequence in the preceding table was used, except the vacuum was 6 torrin Stages 6 and 7. For Example P, the same sequence in the precedingtable was used, except the vacuum was 4 torr in Stages 6 and 7. ForExample Q, the same sequence in the preceding table was used, except thevacuum was 5 torr in Stages 6 and 7.

Camile Sequence for Example H

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 280 90 50 6 5 280 5 25 7110 280 5 25

For Example U and AA, the same sequence in the preceding table was used,except the vacuum was 6 torr in Stages 6 and 7. For Example V and X, thesame sequence in the preceding table was used, except the vacuum was 6torr and stir rate was 15 rpm in Stages 6 and 7. For Example Z, the samesequence in the preceding table was used, except the stir rate was 15rpm in Stages 6 and 7.

Camile Sequence for Example K

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 300 90 50 6 5 300 6 15 7110 300 6 15

For Example M, the same sequence in the preceding table was used, exceptthe vacuum was 8 torr in Stages 6 and 7. For Example N, the samesequence in the preceding table was used, except the vacuum was 7 torrin Stages 6 and 7.

Camile Sequence for Examples S and T

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 5 290 6 25 5 110 290 6 25

The resulting polymers were recovered from the flask, chopped using ahydraulic chopper, and ground to a 6 mm screen size. Samples of eachground polymer were submitted for inherent viscosity in 60/40 (wt/wt)phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at 25° C.,catalyst level (Sn) by x-ray fluorescence, and color (L*, a*, b*) bytransmission spectroscopy. Polymer composition was obtained by 1H NMR.Samples were submitted for thermal stability and melt viscosity testingusing a Rheometrics Mechanical Spectrometer (RMS-800).

Examples AD to AK and AT

The polyesters of these examples were prepared as described above forExamples A to AC, except that the target tin amount in the final polymerwas 150 ppm for examples AD to AK and AT. The following tables describethe temperature/pressure/stir rate sequences controlled by the Camilesoftware for these examples.

Camile Sequence for Examples AD, AF, and AH

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 400 50 5 110 290 400 50 6 5 290 8 507 110 295 8 50

For Example AD, the stirrer was turned to 25 rpm with 95 min left inStage 7.

Camile Sequence for Example AE

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 10 245 760 0 2 5245 760 50 3 30 283 760 50 4 3 283 175 50 5 5 283 5 50 6 5 283 1.2 50 771 285 1.2 50

For Example AK, the same sequence in the preceding table was used,except the time was 75 min in Stage 7.

Camile Sequence for Example AG

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 10 245 760 0 2 5245 760 50 3 30 285 760 50 4 3 285 175 50 5 5 285 5 50 6 5 285 4 50 7220 290 4 50

Camile Sequence for Example AI

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 285 90 50 6 5 285 6 50 770 290 6 50

Camile Sequence for Example AJ

Vacuum Stir Stage Time (min) Temp (° C.) (torr) (rpm) 1 5 245 760 0 2 5245 760 50 3 30 265 760 50 4 3 265 90 50 5 110 290 90 50 6 5 290 6 25 7110 295 6 25

Examples AL to AS

Dimethyl terephthalate, 1,4-cyclohexanedimethanol, and2,2,4,4-tetramethyl-1,3-cyclobutanediol were weighed into a 500-mlsingle neck round bottom flask. The polyesters of this example wereprepared with a 1.2/1 glycol/acid ratio with the entire excess comingfrom the 2,2,4,4-tetramethyl-1,3-cyclobutanediol. Enough dibutyltinoxide catalyst was added to give 300 ppm tin in the final polymer. Theflask was under a 0.2 SCFC nitrogen purge with vacuum reductioncapability. The flask was immersed in a Belmont metal bath at 200° C.and stirred at 200 RPM after the reactants had melted. After about 2.5hours, the temperature was raised to 210° C. and these conditions wereheld for an additional 2 hours. The temperature was raised to 285° C.(in approximately 25 minutes) and the pressure was reduced to 0.3 mm ofHg over a period of 5 minutes. The stirring was reduced as the viscosityincreased, with 15 RPM being the minimum stirring used. The totalpolymerization time was varied to attain the target inherentviscosities. After the polymerization was complete, the Belmont metalbath was lowered and the polymer was allowed to cool to below its glasstransition temperature. After about 30 minutes, the flask was reimmersedin the Belmont metal bath (the temperature had been increased to 295° C.during this 30 minute wait) and the polymer mass was heated until itpulled away from the glass flask. The polymer mass was stirred at midlevel in the flask until the polymer had cooled. The polymer was removedfrom the flask and ground to pass a 3 mm screen. Variations to thisprocedure were made to produce the copolyesters described below with atargeted composition of 45 mol %.

Inherent viscosities were measured as described in the “MeasurementMethods” section above. The compositions of the polyesters weredetermined by ¹H NMR as explained before in the Measurement Methodssection. The glass transition temperatures were determined by DSC, usingthe second heat after quench at a rate of 20° C./min.

The table below shows the experimental data for the polyesters of thisexample. The data shows that an increase in the level of2,2,4,4-tetramethyl-1,3-cyclobutanediol raises the glass transitiontemperature in an almost linear fashion, for a constant inherentviscosity. FIG. 3 also shows the dependence of Tg on composition andinherent viscosity.

TABLE 9 Glass transition temperature as a function of inherent viscosityand composition |_(o) at |_(o) at |_(o) at Exam- mol % % cis IV T_(g)260° C. 275° C. 290° C. ple TMCD TMCD (dL/g) (° C.) (Poise) (Poise)(Poise) A 43.9 72.1 0.46 131 NA NA NA B 44.2 36.4 0.49 118 NA NA NA C 4471.7 0.49 128 NA NA NA D 44.3 36.3 0.51 119 NA NA NA E 46.1 46.8 0.51125 NA NA NA F 43.6 72.1 0.52 128 NA NA NA G 43.6 72.3 0.54 127 NA NA NAH 46.4 46.4 0.54 127 NA NA NA I 45.7 47.1 0.55 125 NA NA NA J 44.4 35.60.55 118 NA NA NA K 45.2 46.8 0.56 124 NA NA NA L 43.8 72.2 0.56 129 NANA NA M 45.8 46.4 0.56 124 NA NA NA N 45.1 47.0 0.57 125 NA NA NA O 45.246.8 0.57 124 NA NA NA P 45 46.7 0.57 125 NA NA NA Q 45.1 47.1 0.58 127NA NA NA R 44.7 35.4 0.59 123 NA NA NA S 46.1 46.4 0.60 127 NA NA NA T45.7 46.8 0.60 129 NA NA NA U 46 46.3 0.62 128 NA NA NA V 45.9 46.3 0.62128 NA NA NA X 45.8 46.1 0.63 128 NA NA NA Y 45.6 50.7 0.63 128 NA NA NAZ 46.2 46.8 0.65 129 NA NA NA AA 45.9 46.2 0.66 128 NA NA NA AB 45.246.4 0.66 128 NA NA NA AC 45.1 46.5 0.68 129 NA NA NA AD 46.3 52.4 0.52NA NA NA NA AE 45.7 50.9 0.54 NA NA NA NA AF 46.3 52.6 0.56 NA NA NA NAAG 46 50.6 0.56 NA NA NA NA AH 46.5 51.8 0.57 NA NA NA NA AI 45.6 51.20.58 NA NA NA NA AJ 46 51.9 0.58 NA NA NA NA AK 45.5 51.2 0.59 NA NA NANA AL 45.8 50.1 0.624 125 NA NA 7696 AM 45.7 49.4 0.619 128 NA NA 7209AN 46.2 49.3 0.548 124 NA NA 2348 AP 45.9 49.5 0.72 128 76600 4026019110  AQ 46.0 50 0.71 131 68310 32480 17817  AR 46.1 49.6 0.383 117 NANA  387 AS 45.6 50.5 0.325 108 NA NA NA AT 47.2 NA 0.48 NA NA NA NA NA =Not available

Example 10

This example illustrates the effect of the predominance of the type of2,2,4,4-tetramethyl-1,3-cyclobutanediol isomer (cis or trans) on theglass transition temperature of the polyester.

Dimethyl terephthalate, 1,4-cyclohexanedimethanol, and2,2,4,4-tetramethyl-1,3-cyclobutanediol were weighed into a 500-mlsingle neck round bottom flask. The polyesters of this example wereprepared with a 1.2/1 glycol/acid ratio with the entire excess comingfrom the 2,2,4,4-tetramethyl-1,3-cyclobutanediol. Enough dibutyltinoxide catalyst was added to give 300 ppm tin in the final polymer. Theflask was under a 0.2 SCFC nitrogen purge with vacuum reductioncapability. The flask was immersed in a Belmont metal bath at 200° C.and stirred at 200 RPM after the reactants had melted. After about 2.5hours, the temperature was raised to 210° C. and these conditions wereheld for an additional 2 hours. The temperature was raised to 285° C.(in approximately 25 minutes) and the pressure was reduced to 0.3 mm ofHg over a period of 5 minutes. The stirring was reduced as the viscosityincreased, with 15 RPM being the minimum stirring used. The totalpolymerization time was varied to attain the target inherentviscosities. After the polymerization was complete, the Belmont metalbath was lowered and the polymer was allowed to cool to below its glasstransition temperature. After about 30 minutes, the flask was reimmersedin the Belmont metal bath (the temperature had been increased to 295° C.during this 30 minute wait) and the polymer mass was heated until itpulled away from the glass flask. The polymer mass was stirred at midlevel in the flask until the polymer had cooled. The polymer was removedfrom the flask and ground to pass a 3 mm screen. Variations to thisprocedure were made to produce the copolyesters described below with atargeted composition of 45 mol %.

Inherent viscosities were measured as described in the “MeasurementMethods” section above. The compositions of the polyesters weredetermined by ¹H NMR as explained before in the Measurement Methodssection. The glass transition temperatures were determined by DSC, usingthe second heat after quench at a rate of 20° C./min.

The table below shows the experimental data for the polyesters of thisExample. The data shows that cis 2,2,4,4-tetramethyl-1,3-cyclobutanediolis approximately twice as effective as trans2,2,4,4-tetramethyl-1,3-cyclobutanediol at increasing the glasstransition temperature for a constant inherent viscosity.

TABLE 10 Effect of 2,2,4,4-tetramethyl-1,3-cyclobutanediol cis/transcomposition on T_(g) Ex- η_(o) at η_(o) □at η_(o) at am- mol % IV T_(g)260° C. 275° C. 290° C. % cis ple TMCD (dL/g) (° C.) (Poise) (Poise)(Poise) TMCD A 45.8 0.71 119 N.A. N.A. N.A. 4.1 B 43.2 0.72 122 N.A.N.A. N.A. 22.0 C 46.8 0.57 119 26306 16941 6601 22.8 D 43.0 0.67 12555060 36747 14410  23.8 E 43.8 0.72 127 101000  62750 25330  24.5 F 45.90.533 119 11474  6864 2806 26.4 G 45.0 0.35 107 N.A. N.A. N.A. 27.2 H41.2 0.38 106 1214  757 N.A. 29.0 I 44.7 0.59 123 N.A. N.A. N.A. 35.4 J44.4 0.55 118 N.A. N.A. N.A. 35.6 K 44.3 0.51 119 N.A. N.A. N.A. 36.3 L44.0 0.49 128 N.A. N.A. N.A. 71.7 M 43.6 0.52 128 N.A. N.A. N.A. 72.1 N43.6 0.54 127 N.A. N.A. N.A. 72.3 O 41.5 0.58 133 15419 10253 4252 88.7P 43.8 0.57 135 16219 10226 4235 89.6 Q 41.0 0.33 120  521  351 226190.4 R 43.0 0.56 134 N.A. N.A. N.A. 90.6 S 43.0 0.49 132  7055  46202120 90.6 T 43.1 0.55 134 12970  8443 3531 91.2 U 45.9 0.52 137 N.A.N.A. N.A. 98.1 NA = not available

Example 11

This example illustrates the preparation of a copolyester containing 100mol % dimethyl terephthalate residues, 55 mol %1,4-cyclohexanedimethanol residues, and 45 mol %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues.

A mixture of 97.10 g (0.5 mol) dimethyl terephthalate, 52.46 g (0.36mol) 1,4-cyclohexanedimethanol, 34.07 g (0.24 mol)2,2,4,4-tetramethyl-1,3-cyclobutanediol, and 0.0863 g (300 ppm) dibutyltin oxide was placed in a 500-milliliter flask equipped with an inletfor nitrogen, a metal stirrer, and a short distillation column. Theflask was placed in a Wood's metal bath already heated to 200° C. Thecontents of the flask were heated at 200° C. for 1 hour and then thetemperature was increased to 210° C. The reaction mixture was held at210° C. for 2 hours and then heated up to 290° C. in 30 minutes. Once at290° C., a vacuum of 0.01 psig was gradually applied over the next 3 to5 minutes. Full vacuum (0.01 psig) was maintained for a total time ofabout 45 minutes to remove excess unreacted diols. A high meltviscosity, visually clear and colorless polymer was obtained with aglass transition temperature of 125° C. and an inherent viscosity of0.64 dl/g.

Example 12 Comparative Example

This example illustrates that a polyester based on 100%2,2,4,4-tetramethyl-1,3-cyclobutanediol has a slow crystallizationhalf-time.

A polyester based solely on terephthalic acid and2,2,4,4-tetramethyl-1,3-cyclobutanediol was prepared in a method similarto the method described in Example 1A with the properties shown on Table11. This polyester was made with 300 ppm dibutyl tin oxide. Thetrans/cis ratio of the 2,2,4,4-tetramethyl-1,3-cyclobutanediol was65/35.

Films were pressed from the ground polymer at 320° C. Crystallizationhalf-time measurements from the melt were made at temperatures from 220to 250° C. at 10° C. increments and are reported in Table 11. Thefastest crystallization half-time for the sample was taken as theminimum value of crystallization half-time as a function of temperature.The fastest crystallization half-time of this polyester is around 1300minutes. This value contrasts with the fact that the polyester (PCT)based solely on terephthalic acid and 1,4-cyclohexanedimethanol (nocomonomer modification) has an extremely short crystallization half-time(<1 min) as shown in FIG. 1.

TABLE 11 Crystallization Half-times (min) at at at at Comonomer IV T_(g)T_(max) 220° C. 230° C. 240° C. 250° C. (mol %) (dl/g) (° C.) (° C.)(min) (min) (min) (min) 100 mol % F 0.63 170.0 330 3291 3066 1303 1888where: F is 2,2,4,4-Tetramethyl-1,3-cyclobutanediol (65/35 Trans/Cis)

Example 13

Sheets comprising a polyester that had been prepared with a targetcomposition of 100 mole % terephthalic acid residues, 80 mole %1,4-cyclohexanedimethanol residues, and 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues were produced using a3.5 inch single screw extruder. A sheet was extruded continuously,gauged to a thickness of 177 mil and then various sheets were sheared tosize. Inherent viscosity and glass transition temperature were measuredon one sheet. The sheet inherent viscosity was measured to be 0.69 dl/g.The glass transition temperature of the sheet was measured to be 106° C.Sheets were then conditioned at 50% relative humidity and 60° C. for 2weeks. Sheets were subsequently thermoformed into a female mold having adraw ratio of 2.5:1 using a Brown thermoforming machine. Thethermoforming oven heaters were set to 70/60/60% output using top heatonly. Sheets were left in the oven for various amounts of time in orderto determine the effect of sheet temperature on the part quality asshown in the table below. Part quality was determined by measuring thevolume of the thermoformed part, calculating the draw, and visuallyinspecting the thermoformed part. The draw was calculated as the partvolume divided by the maximum part volume achieved in this set ofexperiments (Example G). The thermoformed part was visually inspectedfor any blisters and the degree of blistering rated as none (N), low(L), or high (H). The results below demonstrate that these thermoplasticsheets with a glass transition temperature of 106° C. can bethermoformed under the conditions shown below, as evidenced by thesesheets having at least 95% draw and no blistering, without predrying thesheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 86 145 50164 N B 100 150 500 63 N C 118 156 672 85 N D 135 163 736 94 N E 143 166760 97 N F 150 168 740 94 L G 159 172 787 100 L

Example 14

Sheets comprising a polyester that had been prepared with a targetcomposition of 100 mole % terephthalic acid residues, 80 mole %1,4-cyclohexanedimethanol residues, and 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol residues were produced using a3.5 inch single screw. A sheet was extruded continuously, gauged to athickness of 177 mil and then various sheets were sheared to size.Inherent viscosity and glass transition temperature were measured on onesheet. The sheet inherent viscosity was measured to be 0.69 dl/g. Theglass transition temperature of the sheet was measured to be 106° C.Sheets were then conditioned at 100% relative humidity and 25° C. for 2weeks. Sheets were subsequently thermoformed into a female mold having adraw ratio of 2.5:1 using a Brown thermoforming machine. Thethermoforming oven heaters were set to 60/40/40% output using top heatonly. Sheets were left in the oven for various amounts of time in orderto determine the effect of sheet temperature on the part quality asshown in the table below. Part quality was determined by measuring thevolume of the thermoformed part, calculating the draw, and visuallyinspecting the thermoformed part. The draw was calculated as the partvolume divided by the maximum part volume achieved in this set ofexperiments (Example G). The thermoformed part was visually inspectedfor any blisters and the degree of blistering rated as none (N), low(L), or high (H). The results below demonstrate that these thermoplasticsheets with a glass transition temperature of 106° C. can bethermoformed under the conditions shown below, as evidenced by theproduction of sheets having at least 95% draw and no blistering, withoutpredrying the sheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 141 154 39453 N B 163 157 606 82 N C 185 160 702 95 N D 195 161 698 95 N E 215 163699 95 L F 230 168 705 96 L G 274 174 737 100 H H 275 181 726 99 H

Example 15 Comparative Example

Sheets consisting of Kelvx 201 were produced using a 3.5 inch singlescrew extruder. Kelvx is a blend consisting of 69.85% PCTG (Eastar fromEastman Chemical Co. having 100 mole % terephthalic acid residues, 62mole % 1,4-cyclohexanedimethanol residues, and 38 mole % ethylene glycolresidues); 30% PC (bisphenol A polycarbonate); and 0.15% Weston 619(stabilizer sold by Crompton Corporation). A sheet was extrudedcontinuously, gauged to a thickness of 177 mil and then various sheetswere sheared to size. The glass transition temperature was measured onone sheet and was 100° C. Sheets were then conditioned at 50% relativehumidity and 60° C. for 2 weeks. Sheets were subsequently thermoformedinto a female mold having a draw ratio of 2.5:1 using a Brownthermoforming machine. The thermoforming oven heaters were set to70/60/60% output using top heat only. Sheets were left in the oven forvarious amounts of time in order to determine the effect of sheettemperature on the part quality as shown in the table below. Partquality was determined by measuring the volume of the thermoformed part,calculating the draw, and visually inspecting the thermoformed part. Thedraw was calculated as the part volume divided by the maximum partvolume achieved in this set of experiments (Example E). The thermoformedpart was visually inspected for any blisters and the degree ofblistering rated as none (N), low (L), or high (H). The results belowdemonstrate that these thermoplastic sheets with a glass transitiontemperature of 100° C. can be thermoformed under the conditions shownbelow, as evidenced by the production of sheets having at least 95% drawand no blistering, without predrying the sheets prior to thermoforming.

Example 16 Comparative Example

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 90 146 58275 N B 101 150 644 83 N C 111 154 763 98 N D 126 159 733 95 N E 126 159775 100 N F 141 165 757 98 N G 148 168 760 98 L

Sheets consisting of Kelvx 201 were produced using a 3.5 inch singlescrew extruder. A sheet was extruded continuously, gauged to a thicknessof 177 mil and then various sheets were sheared to size. The glasstransition temperature was measured on one sheet and was 100° C. Sheetswere then conditioned at 100% relative humidity and 25° C. for 2 weeks.Sheets were subsequently thermoformed into a female mold having a drawratio of 2.5:1 using a Brown thermoforming machine. The thermoformingoven heaters were set to 60/40/40% output using top heat only. Sheetswere left in the oven for various amounts of time in order to determinethe effect of sheet temperature on the part quality as shown in thetable below. Part quality was determined by measuring the volume of thethermoformed part, calculating the draw, and visually inspecting thethermoformed part. The draw was calculated as the part volume divided bythe maximum part volume achieved in this set of experiments (Example H).The thermoformed part was visually inspected for any blisters and thedegree of blistering rated as none (N), low (L), or high (H). Theresults below demonstrate that these thermoplastic sheets with a glasstransition temperature of 100° C. can be thermoformed under theconditions shown below, as evidenced by the production of sheets havinggreater than 95% draw and no blistering, without predrying the sheetsprior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 110 143 18525 N B 145 149 529 70 N C 170 154 721 95 N D 175 156 725 96 N E 185 157728 96 N F 206 160 743 98 L G 253 NR 742 98 H H 261 166 756 100 H NR =Not recorded

Example 17 Comparative Example

Sheets consisting of PCTG 25976 (100 mole % terephthalic acid residues,62 mole % 1,4-cyclohexanedimethanol residues, and 38 mole % ethyleneglycol residues) were produced using a 3.5 inch single screw extruder. Asheet was extruded continuously, gauged to a thickness of 118 mil andthen various sheets were sheared to size. The glass transitiontemperature was measured on one sheet and was 87° C. Sheets were thenconditioned at 50% relative humidity and 60° C. for 4 weeks. Themoisture level was measured to be 0.17 wt %. Sheets were subsequentlythermoformed into a female mold having a draw ratio of 2.5:1 using aBrown thermoforming machine. The thermoforming oven heaters were set to70/60/60% output using top heat only. Sheets were left in the oven forvarious amounts of time in order to determine the effect of sheettemperature on the part quality as shown in the table below. Partquality was determined by measuring the volume of the thermoformed part,calculating the draw, and visually inspecting the thermoformed part. Thedraw was calculated as the part volume divided by the maximum partvolume achieved in this set of experiments (Example A). The thermoformedpart was visually inspected for any blisters and the degree ofblistering rated as none (N), low (L), or high (H). The results belowdemonstrate that these thermoplastic sheets with a glass transitiontemperature of 87° C. can be thermoformed under the conditions shownbelow, as evidenced by the production of sheets having greater than 95%draw and no blistering, without predrying the sheets prior tothermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 102 183 816100 N B 92 171 811 99 N C 77 160 805 99 N D 68 149 804 99 N E 55 143 79097 N F 57 138 697 85 N

Example 18 Comparative Example

A miscible blend consisting of 20 wt % Teijin L-1250 polycarbonate (abisphenol-A polycarbonate), 79.85 wt % PCTG 25976, and 0.15 wt % Weston619 was produced using a 1.25 inch single screw extruder. Sheetsconsisting of the blend were then produced using a 3.5 inch single screwextruder. A sheet was extruded continuously, gauged to a thickness of118 mil and then various sheets were sheared to size. The glasstransition temperature was measured on one sheet and was 94° C. Sheetswere then conditioned at 50% relative humidity and 60° C. for 4 weeks.The moisture level was measured to be 0.25 wt %. Sheets weresubsequently thermoformed into a female mold having a draw ratio of2.5:1 using a Brown thermoforming machine. The thermoforming ovenheaters were set to 70/60/60% output using top heat only. Sheets wereleft in the oven for various amounts of time in order to determine theeffect of sheet temperature on the part quality as shown in the tablebelow. Part quality was determined by measuring the volume of thethermoformed part, calculating the draw, and visually inspecting thethermoformed part. The draw was calculated as the part volume divided bythe maximum part volume achieved in this set of experiments (Example A).The thermoformed part was visually inspected for any blisters and thedegree of blistering rated as none (N), low (L), or high (H). Theresults below demonstrate that these thermoplastic sheets with a glasstransition temperature of 94° C. can be thermoformed under theconditions shown below, as evidenced by the production of sheets havinggreater than 95% draw and no blistering, without predrying the sheetsprior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 92 184 844100 H B 86 171 838 99 N C 73 160 834 99 N D 58 143 787 93 N E 55 143 66579 N

Example 19 Comparative Example

A miscible blend consisting of 30 wt % Teijin L-1250 polycarbonate,69.85 wt % PCTG 25976, and 0.15 wt % Weston 619 was produced using a1.25 inch single screw extruder. Sheets consisting of the blend werethen produced using a 3.5 inch single screw extruder. A sheet wasextruded continuously, gauged to a thickness of 118 mil and then varioussheets were sheared to size. The glass transition temperature wasmeasured on one sheet and was 99° C. Sheets were then conditioned at 50%relative humidity and 60° C. for 4 weeks. The moisture level wasmeasured to be 0.25 wt %. Sheets were subsequently thermoformed into afemale mold having a draw ratio of 2.5:1 using a Brown thermoformingmachine. The thermoforming oven heaters were set to 70/60/60% outputusing top heat only. Sheets were left in the oven for various amounts oftime in order to determine the effect of sheet temperature on the partquality as shown in the table below. Part quality was determined bymeasuring the volume of the thermoformed part, calculating the draw, andvisually inspecting the thermoformed part. The draw was calculated asthe part volume divided by the maximum part volume achieved in this setof experiments (Example A). The thermoformed part was visually inspectedfor any blisters and the degree of blistering rated as none (N), low(L), or high (H). The results below demonstrate that these thermoplasticsheets with a glass transition temperature of 99° C. can be thermoformedunder the conditions shown below, as evidenced by the production ofsheets having greater than 95% draw and no blistering, without predryingthe sheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 128 194 854100 H B 98 182 831 97 L C 79 160 821 96 N D 71 149 819 96 N E 55 145 78592 N F 46 143 0 0 NA G 36 132 0 0 NA NA = not applicable. A value ofzero indicates that the sheet was not formed because it did not pullinto the mold (likely because it was too cold).

Example 20 Comparative Example

A miscible blend consisting of 40 wt % Teijin L-1250 polycarbonate,59.85 wt % PCTG 25976, and 0.15 wt % Weston 619 was produced using a1.25 inch single screw extruder. Sheets consisting of the blend werethen produced using a 3.5 inch single screw extruder. A sheet wasextruded continuously, gauged to a thickness of 118 mil and then varioussheets were sheared to size. The glass transition temperature wasmeasured on one sheet and was 105° C. Sheets were then conditioned at50% relative humidity and 60° C. for 4 weeks. The moisture level wasmeasured to be 0.265 wt %. Sheets were subsequently thermoformed into afemale mold having a draw ratio of 2.5:1 using a Brown thermoformingmachine. The thermoforming oven heaters were set to 70/60/60% outputusing top heat only. Sheets were left in the oven for various amounts oftime in order to determine the effect of sheet temperature on the partquality as shown in the table below. Part quality was determined bymeasuring the volume of the thermoformed part, calculating the draw, andvisually inspecting the thermoformed part. The draw was calculated asthe part volume divided by the maximum part volume achieved in this setof experiments (Examples 8A to 8E). The thermoformed part was visuallyinspected for any blisters and the degree of blistering rated as none(N), low (L), or high (H). The results below demonstrate that thesethermoplastic sheets with a glass transition temperature of 105° C. canbe thermoformed under the conditions shown below, as evidenced by theproduction of sheets having greater than 95% draw and no blistering,without predrying the sheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 111 191 828100 H B 104 182 828 100 H C 99 179 827 100 N D 97 177 827 100 N E 78 160826 100 N F 68 149 759 92 N G 65 143 606 73 N

Example 21 Comparative Example

A miscible blend consisting of 50 wt % Teijin L-1250 polycarbonate,49.85 wt % PCTG 25976, and 0.15 wt % Weston 619 was produced using a1.25 inch single screw extruder. A sheet was extruded continuously,gauged to a thickness of 118 mil and then various sheets were sheared tosize. The glass transition temperature was measured on one sheet and was111° C. Sheets were then conditioned at 50% relative humidity and 60° C.for 4 weeks. The moisture level was measured to be 0.225 wt %. Sheetswere subsequently thermoformed into a female mold having a draw ratio of2.5:1 using a Brown thermoforming machine. The thermoforming ovenheaters were set to 70/60/60% output using top heat only. Sheets wereleft in the oven for various amounts of time in order to determine theeffect of sheet temperature on the part quality as shown in the tablebelow. Part quality was determined by measuring the volume of thethermoformed part, calculating the draw, and visually inspecting thethermoformed part. The draw was calculated as the part volume divided bythe maximum part volume achieved in this set of experiments (Examples Ato D). The thermoformed part was visually inspected for any blisters andthe degree of blistering rated as none (N), low (L), or high (H). Theresults below demonstrate that these thermoplastic sheets with a glasstransition temperature of 111° C. can be thermoformed under theconditions shown below, as evidenced by the production of sheets havinggreater than 95% draw and no blistering, without predrying the sheetsprior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 118 192 815100 H B 99 182 815 100 H C 97 177 814 100 L D 87 171 813 100 N E 80 160802 98 N F 64 154 739 91 N G 60 149 0 0 NA NA = not applicable. A valueof zero indicates that the sheet was not formed because it did not pullinto the mold (likely because it was too cold).

Example 22 Comparative Example

A miscible blend consisting of 60 wt % Teijin L-1250 polycarbonate,39.85 wt % PCTG 25976, and 0.15 wt % Weston 619 was produced using a1.25 inch single screw extruder. Sheets consisting of the blend werethen produced using a 3.5 inch single screw extruder. A sheet wasextruded continuously, gauged to a thickness of 118 mil and then varioussheets were sheared to size. The glass transition temperature wasmeasured on one sheet and was 117° C. Sheets were then conditioned at50% relative humidity and 60° C. for 4 weeks. The moisture level wasmeasured to be 0.215 wt %. Sheets were subsequently thermoformed into afemale mold having a draw ratio of 2.5:1 using a Brown thermoformingmachine. The thermoforming oven heaters were set to 70/60/60% outputusing top heat only. Sheets were left in the oven for various amounts oftime in order to determine the effect of sheet temperature on the partquality as shown in the table below. Part quality was determined bymeasuring the volume of the thermoformed part, calculating the draw, andvisually inspecting the thermoformed part. The draw was calculated asthe part volume divided by the maximum part volume achieved in this setof experiments (Example A). The thermoformed part was visually inspectedfor any blisters and the degree of blistering rated as none (N), low(L), or high (H). The results below demonstrate that these thermoplasticsheets with a glass transition temperature of 117° C. cannot bethermoformed under the conditions shown below, as evidenced by theinability to produce sheets having greater than 95% draw and noblistering, without predrying the sheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 114 196 813100 H B 100 182 804 99 H C 99 177 801 98 L D 92 171 784 96 L E 82 168727 89 L F 87 166 597 73 N

Example 23 Comparative Example

A miscible blend consisting of 65 wt % Teijin L-1250 polycarbonate,34.85 wt % PCTG 25976, and 0.15 wt % Weston 619 was produced using a1.25 inch single screw extruder. Sheets consisting of the blend werethen produced using a 3.5 inch single screw extruder. A sheet wasextruded continuously, gauged to a thickness of 118 mil and then varioussheets were sheared to size. The glass transition temperature wasmeasured on one sheet and was 120° C. Sheets were then conditioned at50% relative humidity and 60° C. for 4 weeks. The moisture level wasmeasured to be 0.23 wt %. Sheets were subsequently thermoformed into afemale mold having a draw ratio of 2.5:1 using a Brown thermoformingmachine. The thermoforming oven heaters were set to 70/60/60% outputusing top heat only. Sheets were left in the oven for various amounts oftime in order to determine the effect of sheet temperature on the partquality as shown in the table below. Part quality was determined bymeasuring the volume of the thermoformed part, calculating the draw, andvisually inspecting the thermoformed part. The draw was calculated asthe part volume divided by the maximum part volume achieved in this setof experiments (Example A). The thermoformed part was visually inspectedfor any blisters and the degree of blistering rated as none (N), low(L), or high (H). The results below demonstrate that these thermoplasticsheets with a glass transition temperature of 120° C. cannot bethermoformed under the conditions shown below, as evidenced by theinability to produce sheets having greater than 95% draw and noblistering, without predrying the sheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 120 197 825100 H B 101 177 820 99 H C 95 174 781 95 L D 85 171 727 88 L E 83 166558 68 L

Example 24 Comparative Example

A miscible blend consisting of 70 wt % Teijin L-1250 polycarbonate,29.85 wt % PCTG 25976, and 0.15 wt % Weston 619 was produced using a1.25 inch single screw extruder. Sheets consisting of the blend werethen produced using a 3.5 inch single screw extruder. A sheet wasextruded continuously, gauged to a thickness of 118 mil and then varioussheets were sheared to size. The glass transition temperature wasmeasured on one sheet and was 123° C. Sheets were then conditioned at50% relative humidity and 60° C. for 4 weeks. The moisture level wasmeasured to be 0.205 wt %. Sheets were subsequently thermoformed into afemale mold having a draw ratio of 2.5:1 using a Brown thermoformingmachine. The thermoforming oven heaters were set to 70/60/60% outputusing top heat only. Sheets were left in the oven for various amounts oftime in order to determine the effect of sheet temperature on the partquality as shown in the table below. Part quality was determined bymeasuring the volume of the thermoformed part, calculating the draw, andvisually inspecting the thermoformed part. The draw was calculated asthe part volume divided by the maximum part volume achieved in this setof experiments (Examples A and B). The thermoformed part was visuallyinspected for any blisters and the degree of blistering rated as none(N), low (L), or high (H). The results below demonstrate that thesethermoplastic sheets with a glass transition temperature of 123° C.cannot be thermoformed under the conditions shown below, as evidenced bythe inability to produce sheets having greater than 95% draw and noblistering, without predrying the sheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 126 198 826100 H B 111 188 822 100 H C 97 177 787 95 L D 74 166 161 19 L E 58 154 00 NA F 48 149 0 0 NA NA = not applicable. A value of zero indicates thatthe sheet was not formed because it did not pull into the mold (likelybecause it was too cold).

Example 25 Comparative Example

Sheets consisting of Teijin L-1250 polycarbonate were produced using a3.5 inch single screw extruder. A sheet was extruded continuously,gauged to a thickness of 118 mil and then various sheets were sheared tosize. The glass transition temperature was measured on one sheet and was149° C. Sheets were then conditioned at 50% relative humidity and 60° C.for 4 weeks. The moisture level was measured to be 0.16 wt %. Sheetswere subsequently thermoformed into a female mold having a draw ratio of2.5:1 using a Brown thermoforming machine. The thermoforming ovenheaters were set to 70/60/60% output using top heat only. Sheets wereleft in the oven for various amounts of time in order to determine theeffect of sheet temperature on the part quality as shown in the tablebelow. Part quality was determined by measuring the volume of thethermoformed part, calculating the draw and visually inspecting thethermoformed part. The draw was calculated as the part volume divided bythe maximum part volume achieved in this set of experiments (Example A).The thermoformed part was visually inspected for any blisters and thedegree of blistering rated as none (N), low (L), or high (H). Theresults below demonstrate that these thermoplastic sheets with a glasstransition temperature of 149° C. cannot be thermoformed under theconditions shown below, as evidenced by the inability to produce sheetshaving greater than 95% draw and no blistering, without predrying thesheets prior to thermoforming.

Thermoforming Conditions Part Quality Sheet Part Heat Time TemperatureVolume Blisters Example (s) (° C.) (mL) Draw (%) (N, L, H) A 152 216 820100 H B 123 193 805 98 H C 113 191 179 22 H D 106 188 0 0 H E 95 182 0 0NA F 90 171 0 0 NA NA = not applicable. A value of zero indicates thatthe sheet was not formed because it did not pull into the mold (likelybecause it was too cold).

It can be clearly seen from a comparison of the data in the aboverelevant working examples that the polyesters of the present inventionoffer a definite advantage over the commercially available polyesterswith regard to glass transition temperature, density, slowcrystallization rate, melt viscosity, and toughness.

The invention has been described in detail with reference to theembodiments disclosed herein, but it will be understood that variationsand modifications can be effected within the spirit and scope of theinvention.

What is claimed is:
 1. A bottle comprising at least one polyestercomposition comprising at least one polyester which comprises: (a) adicarboxylic acid component comprising: i) 70 to 100 mole % ofterephthalic acid residues; ii) 0 to 30 mole % of aromatic dicarboxylicacid residues having up to 20 carbon atoms; and iii) 0 to 10 mole % ofaliphatic dicarboxylic acid residues having up to 16 carbon atoms; and(b) a glycol component comprising: i) 30 to 40 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and ii) 60 to 70 mole% of 1,4-cyclohexanedimethanol residues, wherein the total mole % ofsaid dicarboxylic acid component is 100 mole %, and the total mole % ofsaid glycol component is 100 mole %; wherein the inherent viscosity ofsaid polyester is from 0.50 to 0.68 dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at 25° C.;and wherein said polyester has a Tg of from 100 to 140° C.; wherein saidpolyester has a notched Izod impact strength of at least 7.5 ft-lb/inchat 23° C. according to ASTM D256 with a 10-mil notch in a ⅛-inch thickbar; wherein the melt viscosity of said polyester is less than 10,000poise as measured at 1 radian/second on a rotary melt rheometer at 290°C.; and wherein said polyester composition contains no polycarbonate. 2.The bottle of claim 1, wherein the inherent viscosity of said polyesteris from 0.60 to 0.68 dL/g.
 3. The bottle of claim 1, wherein saidpolyester has a Tg of 100 to 130° C.
 4. The bottle of claim 1 whereinsaid polyester has a Tg of 100 to 120° C.
 5. The bottle of claim 1,wherein said polyester has a Tg of 110 to 140° C.
 6. The bottle of claim1, wherein said polyester has a Tg of 110 to 130° C.
 7. The bottle ofclaim 1, wherein the glycol component of said polyester comprises 30 to35 mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol and 65 to 70 mole %1,4-cyclohexanedimethanol.
 8. The bottle of claim 1, wherein the glycolcomponent of said polyester comprises 35 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 60 to 65 mole %1,4-cyclohexanedimethanol.
 9. The bottle of claim 1, wherein thedicarboxylic acid component comprises 80 to 100 mole % of terephthalicacid residues.
 10. The bottle of claim 1, wherein the dicarboxylic acidcomponent comprises 90 to 100 mole % of terephthalic acid residues. 11.The bottle of claim 1, wherein the dicarboxylic acid component comprises100 mole % of terephthalic acid residues.
 12. The bottle of claim 1,wherein said polyester comprises 1,3-propanediol residues,1,4-butanediol residues, or a mixture thereof.
 13. The bottle of claim1, wherein said 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues are amixture comprising 40 mole % ofcis-2,2,4,4-tetramethyl-1,3-cyclobutanediol residues or greater and 60mole % or less of trans-2,2,4,4-tetramethyl-1,3-cyclobutanediolresidues.
 14. The bottle of claim 1, wherein said2,2,4,4-tetramethyl-1,3-cyclobutanediol residues are a mixturecomprising greater than 50 mole % ofcis-2,2,4,4-tetramethyl-1,3-cyclobutanediol residues and less than 50mole % of trans-2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. 15.The bottle of claim 1, wherein said2,2,4,4-tetramethyl-1,3-cyclobutanediol is a mixture comprising greaterthan 55 mole % of cis-2,2,4,4-tetramethyl-1,3-cyclobutanediol residuesand less than 45 mole % of trans-2,2,4,4-tetramethyl-1,3-cyclobutanediolresidues.
 16. The bottle of claim 1, wherein said polyester compositioncomprises at least one polymer chosen from at least one of thefollowing: nylons; polyesters other than those of claim 1; polyamides;polystyrene; polystyrene copolymers; styrene acrylonitrile copolymers;acrylonitrile butadiene styrene copolymers; poly(methylmethacrylate),acrylic copolymers; poly(ether-imides); polyphenylene oxides,poly(phenylene oxide)/polystyrene blends; polyphenylene sulfides;polyphenylene sulfide/sulfones; polysulfones; polysulfone ethers; andpoly(ether-ketones) of aromatic dihydroxy compounds; or mixturesthereof.
 17. The bottle of claim 1, wherein said polyester comprisesresidues of at least one branching agent for said polyester.
 18. Thebottle of claim 1, wherein said polyester comprises residues of at leastone branching agent in an amount of 0.01 to 10 mole % based on the totalmole % of diacid residues or diol residues in the polyester.
 19. Thebottle of claim 1, wherein the melt viscosity of said polyester is lessthan 6,000 poise as measured at 1 radian/second on a rotary meltrheometer at 290° C.
 20. The bottle of claim 1, wherein said polyesterhas a crystallization half-time of greater than 5 minutes at 170° C. 21.The bottle of claim 1, wherein said polyester has a crystallizationhalf-time of greater than 1,000 minutes at 170° C.
 22. The bottle ofclaim 1, wherein said polyester has a crystallization half-time ofgreater than 10,000 minutes at 170° C.
 23. The bottle of claim 1,wherein said polyester composition has a density of 1.10 to less than1.2 g/ml at 23° C.
 24. The bottle of claim 1, wherein said polyestercomposition comprises at least one thermal stabilizer or reactionproducts thereof.
 25. The bottle of claim 1, wherein the yellownessindex of said polyester according to ASTM D-1925 is less than
 50. 26.The bottle of claim 1, wherein said polyester has a notched Izod impactstrength of at least 10 ft-lbs/in at 23° C. according to ASTM D256 witha 10-mil notch in a ⅛-inch thick bar.
 27. The bottle of claim 1, whereinsaid bottle is a large commercial water bottle having a weight from 200to 800 grams.
 28. The bottle of claim 26, wherein said bottle is chosenfrom at least one of the following: two liter bottles, 20 ounce bottles,16.9 ounce bottles; medical bottles; personal care bottles, carbonatedsoft drink bottles; hot fill bottles; water bottles: alcoholic beveragebottles; or bottles comprising at least one handle.
 29. The bottle ofclaim 26, wherein said alcoholic beverage bottles are chosen from beerbottles or wine bottles.
 30. A bottle comprising at least one polyestercomposition comprising at least one polyester which comprises: (a) adicarboxylic acid component comprising: i) 70 to 100 mole % ofterephthalic acid residues: ii) 0 to 30 mole % of aromatic dicarboxylicacid residues having up to 20 carbon atoms; and iii) 0 to 10 mole % ofaliphatic dicarboxylic acid residues having up to 16 carbon atoms; and(b) a glycol component comprising: i) 30 to 40 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and ii) 60 to 70 mole% of 1,4-cyclohexanedimethanol residues, (c) residues of at least onebranching agent; wherein the total mole % of the dicarboxylic acidcomponent is 100 mole %, and the total mole % of the glycol component is100 mole %: wherein the inherent viscosity of said polyester is from0.50 to 0.68 dL/g as determined in 60/40 (wt/wt)phenol/tetrachloroethaneat a concentration of 0.5 g/100 ml at 25° C.; and wherein said polyesterhas a Tg of 100 to 140° C. wherein said polyester has a notched Izodimpact strength of at least 7.5 ft-lb/inch at 23° C. according to ASTMD256 with a 10-mil notch in a ⅛-inch thick bar; wherein the meltviscosity of said polyester is less than 10,000 poise as measured at 1radian/second on a rotary melt rheometer at 290° C.; and wherein saidpolyester composition contains no polycarbonate.
 31. The bottle of claim30 wherein the wherein the melt viscosity of the polyester is less than6.000 poise as measured at 1 radian/second (rad/sec) on a rotary meltrheometer at 290° C.
 32. The bottle of claims 1 or 30, wherein thepolyester has a b* value of from 10 to less than 10 and a L* value from50 to 90 according to the L*, a* and b* color system of the CIE(International Commission on Illumination).
 33. The bottle of claim 30,wherein the polyester compositions comprises residues from at least onebranching agent in the amount of 0.01 to 5 mole % based on the totalmole percentage of the diacid residues or diol residues.
 34. The bottleof claim 30, wherein said polyester comprises residues from at least onebranching agent in an amount of 0.1 to 0.7 mole % based on the totalmole percentage of the diacid residues or diol residues.
 35. The bottleof claim 30, wherein said polyester comprises residues from at least onebranching agent selected from trimellitic acid, trimellitic anhydride,pyromellitic dianhydride, trimethylolpropane, glycerol, pentaerythritol,citric acid, tartaric acid, or 3-hydroxyglutaric acid.
 36. The bottle ofclaim 30, wherein said polyester comprises residues from trimelliticanhydride.
 37. The bottle of claims 1 or 30, wherein the polyestercomprises a thermal stabilizer which is a phosphorus compound chosenfrom at least one of phosphoric acid, phosphorous acid, phosphonic acid,phosphinic acid, phosphonous acid, or an ester or salt thereof.
 38. Thebottle of claim 30 wherein the polyester has a notched Izod impactstrength of at least 10 ft-lbs/in at 23° C. according to ASTM D256 witha 10-mil notch in a ⅛-inch thick bar.
 39. The bottle of claims 1 or 30wherein said bottle is chosen from at least one of the following:injection blow molded bottles, injection stretch blow molded bottles,extrusion blow molded bottles, or extrusion stretch blow molded bottles.40. The bottle of claim 30, wherein said bottle is a large commercialwater bottle having a weight from 200 to 800 grams.
 41. The bottle ofclaim 30, wherein said bottle is chosen from at least one of thefollowing: two liter bottles, 20 ounce bottles, 16.9 ounce bottles;medical bottles; personal care bottles, carbonated soft drink bottles;hot fill bottles; water bottles; alcoholic beverage bottles; or bottlescomprising at least one handle.